Welch Allyn 42MTB, 420TB, 42NTB, 42NOB, 42MOB, 4200B User manual

Welch Allyn 42MTB, 420TB, 42NTB, 42NOB, 42MOB, 4200B User manual

Welch Allyn Spot Vital Signs

SYS kPa (mmHg)

DIA kPa (mmHg)

SpO

2

%

/ min

Directions for Use

REF 420 Series

Spot Vital Signs

CAUTION

: United States Federal Law restricts this device to sale by or on the order of a health care practitioner.

Welch Allyn Spot Vital Signs

Directions for Use

ii

Welch Allyn Spot Vital Signs

Copyright 2007 Welch Allyn. All rights are reserved. No one is permitted to reproduce or duplicate, in any form, this manual or any part thereof without permission from Welch Allyn.

Welch Allyn assumes no responsibility for any injury to anyone, or for any illegal or improper use of the product, that may result from failure to use this product in accordance with the instructions, cautions, warnings, or statement of intended use published in this manual.

Welch Allyn®, Spot Vital Signs®, and SureTemp® are registered trademarks of Welch Allyn.

LNCS™, SET®, LNOP®, and Masimo® are registered trademarks of, Masimo Corporation. Possession or purchase of a Masimo SpO

2

-equipped device does not convey any express or implied license to use the device with unauthorized sensors or cables which would, alone or in combination with this device, fall within the scope of one or more of the patents relating to this device.

Nellcor® and Oxi-Max® are registered trademarks of Nellcor Puritan Bennett Inc.

Software in this product is Copyright 2007 Welch Allyn or its vendors. All rights are reserved. The software is protected by United States of America copyright laws and international treaty provisions applicable worldwide. Under such laws, the licensee is entitled to use the copy of the software incorporated with this instrument as intended in the operation of the product in which it is embedded. The software may not be copied, decompiled, reverse-engineered, disassembled, or otherwise reduced to human-perceivable form. This is not a sale of the software or any copy of the software; all right, title, and ownership of the software remain with Welch Allyn or its vendors.

For information about any Welch Allyn product, call Welch Allyn Technical Support:

USA +1 800 535 6663

+ 1 315 685 4560

Canada +1 800 561 8797

European Call Center +353 46 90 67790

Germany +49 7477 9271 70

Latin America +1 305 669 9003

Singapore +65 6419 8100

United Kingdom +44 207 365 6780

Australia +61 2 9638 3000

+800 074 793

China +86 21 6327 9631

France +33 1 55 69 58 49

Japan +81 3 3219 0071

Netherlands +31 157 505 000

South Africa +27 11 777 7555

Sweden +46 85 853 6551

Reorder No. 4200-87E

Manual Material No. 706272 Ver. C

Welch Allyn

4341 State Street Road

Skaneateles Falls, NY 13153 USA

Printed in USA

Directions for Use

iii

Configuration

After recharging a dead battery or after disconnecting the battery for a few minutes, you must program the

date and time screen. See page 19 for more details.

SYS

(mmHg)

DIA

(mmHg)

/ min

iv

Welch Allyn Spot Vital Signs

Contents

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . iii

1 - Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1

Product Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1

Related Publications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2

Indications/Contraindications for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2

Symbols and Descriptions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3

Safety Warnings and Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

Avertissements et précautions de sécurité . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

Précautions générales . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12

2 - Controls, Indicators, and Connections . . . . . . . . . . . . . . . . . . . . . . 15

Unpacking Checklist . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

Possible Attachments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

Front Panel Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

LCD (Liquid Crystal Display) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

Top, Side, and Rear Panel Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18

3 - Internal Configuration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

4 - Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

Blood Pressure Hose and Cuff Connections. . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

Temperature Probe Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

SpO

2

Sensor Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

Quick Reference/Error Code Card. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

AC Power Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

Charging the Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

Standby Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

5 - Blood Pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

Selecting the Blood Pressure Cuff . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

Reviewing Information from the Last Cycle . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25

Checking the Blood Pressure Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26

6 - Temperature. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

Selecting Temperature Operation Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

Temperature Measurement Range Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . 29

v

vi

Contents Welch Allyn Spot Vital Signs

Normal Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

Monitor Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33

7 - Pulse Oximetry (Sp0

2

). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35

8 - Error Indications and Interpretation . . . . . . . . . . . . . . . . . . . . . . . . 37

Error Codes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37

Causes and Corrective Action. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39

9 - Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43

Patient Population . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43

Blood Pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43

Temperature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43

Pulse Oximetry . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44

Mechanical . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46

Electrical . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46

Environmental. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46

Guidance and Manufacturer’s Declaration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47

Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51

Agency Approvals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51

10 - Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53

Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53

Battery Removal and Replacement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54

Masimo SpO

2

Calibration Check. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55

Nellcor SpO

2

Functional Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55

SpO

2

Accessory Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55

Temperature Calibration Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55

Service Manual/Spare Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56

Service Loaners . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56

Service Policy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56

Technical Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56

11 - Supplies and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57

Latex-Free Blood Pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57

Pulse Oximetry Accessories and Supplies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

Temperature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

Mounting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

Extended Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

Miscellaneous. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61

Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63

Spot . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63

Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63

1

Introduction

This manual is designed to help you understand the capabilities and operation of your

Welch Allyn Spot Vital Signs. The information in this manual includes all options available with the Spot Vital Signs (e.g., SpO

2

, temperature, mobile stand, and wall mount). The applicability of some sections of this manual depends on the configuration of your particular unit. Read this manual thoroughly before attempting to use the device.

REF

4200B

420TB

42MOB

42NOB

42MTB

42NTB

Table 1. Available Versions of Spot Vital Signs

Description

Spot Vital Signs with blood pressure only

Spot Vital Signs with blood pressure and SureTemp thermometer

Spot Vital Signs with blood pressure and Masimo SpO

2

Spot Vital Signs with blood pressure and Nellcor SpO

2

Spot Vital Signs with blood pressure, SureTemp thermometer, and Masimo SpO

2

Spot Vital Signs with blood pressure, SureTemp thermometer, and Nellcor SpO

2

Product Overview

The Welch Allyn Spot Vital Signs non-invasively and automatically measures systolic and diastolic blood pressure, pulse rate, and oxygen saturation (SpO

2

) for adult and pediatric patients. Further, the Welch Allyn Spot Vital Signs measures temperature invasively in natural body orifices (i.e., mouth and rectum).

THE WELCH ALLYN SPOT VITAL SIGNS IS NOT INTENDED FOR USE ON NEONATAL

PATIENTS

.

All blood pressure, pulse, temperature, and SpO

2

values are viewed on a large, easy-toread display.

The rechargeable lead acid battery and variety of mounting accessories make the Welch

Allyn Spot Vital Signs convenient for many locations. You may choose any combination of simultaneous measurement modalities.

The Welch Allyn Spot Vital Signs can be used in a wide variety of health care settings. This includes hospital departments as well as alternate care settings such as physicians’ offices, clinics, and long-term care facilities. The Welch Allyn Spot Vital Signs is not intended for continuous monitoring of patients, nor for use during the transport of a patient. The Welch Allyn Spot Vital Signs is not intended for use in environments that are not supervised by a health care practitioner.

1

2

Welch Allyn Spot Vital Signs

Related Publications

Masimo Directions for Use - for models 42M0B and 42MTB

Nelcor Directions for Use - for models 42N0B and 42NTB

Indications/Contraindications for Use

The Welch Allyn Spot Vital Signs measures blood pressure, pulse rate, temperature, and

SpO

2

of adult and pediatric patients. The device is not designed, sold, nor intended for use other than previously stated.

THE WELCH ALLYN SPOT VITAL SIGNS IS NOT INTENDED FOR USE ON NEONATAL

PATIENTS.

To ensure pediatric blood pressure accuracy and safety, the Welch Allyn Child Print Cuff

(5200-03), the Welch Allyn Small Child Durable One-Piece Cuff (5082-203-3), and the

Welch Allyn Small Child Disposable One-Piece Cuff (5082-93-3) are the smallest cuffs allowed for use with young children and infants. The circumference of the child’s arm must fit within the range markings on the cuff.

The Welch Allyn Spot Vital Signs is FDA cleared to measure the axillary temperature in normal mode for children under the age of 4.

The Welch Allyn Spot Vital Signs is not intended for continuous monitoring and is therefore not defibrillator proof.

Do not leave the device unattended while taking measurements on a patient.

The Welch Allyn Spot Vital Signs should not be used on patients who are linked to heart/ lung machines.

Directions for Use

Symbols and Descriptions

Familiarize all operating personnel with the general safety information in this summary.

Operators will also find specific warnings and cautions throughout the Directions for Use.

Such specific warnings and cautions may not appear here in this summary.

Caution:

Consult manual for additional information.

3

Type BF Equipment

Handle with Care

Transport Temperature

Storage Humidity

+

Pb

Internally Powered, Lead Acid Battery.

Class II Equipment

IPXØ

Not protected against the ingress of water.

Mode of Operation: Continuous

Do not dispose of this product as unsorted municipal waste. Prepare this product for reuse or separate collection as specified by Directive 2002/

96/EC of the European Parliament and the Council of the European

Union on Waste Electronic and Electrical Equipment (WEEE). If this product is contaminated, this directive does not apply.

For more specific disposal information, see www.welchallyn.com/weee, or contact Welch Allyn Customer Service at +44 207 365 6780.

4

Welch Allyn Spot Vital Signs

Safety Warnings and Cautions

All operating personnel should be familiarized with the general safety information in this summary. Specific warnings and cautions are also found throughout this manual. Such specific warnings and cautions may not appear here in this summary.

General Warnings

A warning statement in this manual identifies a condition or practice, which if not corrected or discontinued immediately, could lead to patient injury, illness, or death.

WARNING

The Welch Allyn Spot Vital Signs is designed for use by medical clinicians. Although this manual may illustrate medical spot check techniques, only a trained clinician who knows how to take and interpret a patient’s vital signs should use this system.

WARNING

The information in this manual is a comprehensive guide to the operation of the Welch Allyn Spot Vital Signs. To achieve satisfactory results, you should read the manual thoroughly before attempting to use the device.

WARNING

Spot Vital Signs is not intended to take measurements on neonatal patients. The AAMI SP10:1992 standard defines neonates as children 28 days or less of age if born at term (37 weeks gestation or more); otherwise up to 44 gestational weeks.

WARNING

The Welch Allyn Spot Vital Signs is not defibrillator proof.

WARNING

The Welch Allyn Spot Vital Signs is not intended for continuous monitoring. Do not leave the device unattended while taking measurements on a patient.

WARNING

To ensure patient safety, use only accessories and supplies (i.e., blood pressure cuffs, hoses, temperature probes, SpO

2

sensors, etc.) recommended for or supplied with Spot Vital Signs. Using unapproved accessories with Spot Vital Signs can affect patient and/or operator safety.

WARNING

This device is not suitable for use in the presence of a flammable anesthetic mixture with air or oxygen or nitrous oxide. An explosion may result.

WARNING

Avoid compression of the blood pressure cuff tubing or pressure hose of the Welch Allyn Spot Vital Signs. Compression of the cuff tubing or pressure hose may cause system errors to occur in the device.

WARNING

Care should be taken to prevent water or other fluid from entering any connectors on the device. Should this occur, the connectors should be dried with warm air. All operating functions should then be checked for proper operation.

WARNING

Any Spot Vital Signs which has been dropped or damaged should be checked by qualified service personnel to ensure proper operation prior to use.

Do not use the Welch Allyn Spot Vital Signs if you notice any signs of damage.

Contact the Welch Allyn Customer Service Department for assistance.

WARNING

Every three months, inspect the temperature probe, SpO

2 cord, and accessories for fraying or other damage. Replace as necessary.

Directions for Use

WARNING

There are no user-serviceable parts inside the device other than battery replacement. Refer Spot Vital Signs to the Authorized Service Center.

WARNING

The Spot Vital Signs should not be used on patients who are linked to heart/lung machines.

WARNING

The Spot Vital Signs does not operate effectively on patients who are experiencing convulsions or tremors.

WARNING

This device complies with current required standards for electromagnetic interference and should not present problems to other equipment or be affected by other devices. As a precaution, avoid using this device in close proximity to other equipment.

WARNING

This device is not intended for hand-held use during operation.

WARNING

Welch Allyn recommends leaving the battery in the device, regardless if the device is not used for long periods of time, since there is no hazard of leaving the battery in the device.

WARNING

Do not autoclave.

WARNING

Welch Allyn is not responsible for the integrity of any mounting installation. Welch Allyn recommends that the customer contact their Biomedical

Engineering Department or maintenance service to ensure professional installation for safety and reliability of any mounting accessory.

Blood Pressure Warnings

WARNING

To ensure pediatric blood pressure accuracy and safety, the Welch

Allyn Child Print Cuff (5200-03), the Welch Allyn Small Child Durable One-Piece

Cuff (5082-203-3), and the Welch Allyn Small Child Disposable One-Piece Cuff

(5082-93-3) are the smallest cuffs allowed for use with young children and infants.

The circumference of the child’s arm must fit within the range markings on the cuff.

WARNING

You may experience inaccurate blood pressure measurements if blood pressure cuffs and/or hoses other than those provided by Welch Allyn for the Spot Vital Signs are used.

WARNING

Patients who are experiencing moderate to severe arrhythmias may give inaccurate blood pressure measurements.

WARNING

When several blood pressure measurements are taken on the same patient, it is recommended that the blood pressure cuff site and extremity are checked regularly for possible ischemia, purpura, and/or neuropathy.

WARNING

Do not change the connector(s) on the blood pressure cuff tubing of this device to luer type. Luer type connectors are commonly used in intravenous infusion systems. Using the luer connectors on blood pressure cuff tubing creates the risk that the blood pressure tubing could be mistakenly connected to a patient's intravenous line, resulting in the introduction of air into the patient's circulatory system.

5

6

Welch Allyn Spot Vital Signs

SpO

2

Warnings

WARNING

Only use Spot Vital Signs with Masimo or Nellcor SpO

2

option with

Masimo or Nellcor brand sensors and accessories, respectively. Using the wrong or unapproved sensors or cables may cause improper performance.

WARNING

The SpO

2

sensors and extension cables are intended for use only for pulse oximetry measurements. Do not attempt to connect these cables to a PC or any similar device.

WARNING

Before use, carefully read the sensor’s directions for use, including all warnings, cautions, and instructions.

WARNING

Do not use a damaged sensor or SpO

2

cable. Do not use a sensor with exposed optical components.

WARNING

Tissue damage can be caused by incorrect application or duration of use of an SpO

2

sensor. Inspect the sensor site as directed in the sensor’s

Directions for Use.

WARNING

Do not use the sensors during magnetic resonance imaging (MRI) scanning. Induced current could potentially cause burns. The pulse oximeter may affect the MRI image, and the MRI unit may affect the accuracy of the pulse oximetry measurements.

WARNING

Certain ambient environmental conditions, sensor application errors, and certain patient conditions may affect SpO

2

readings and pulse signal.

WARNING

Do not immerse the sensor or patient cables in water, solvents, or cleaning solutions (the sensors and connections are not waterproof). Do not use irradiation, steam, or ethylene oxide for sterilization.

WARNING

Do not use the SpO

2

cable or power cord to lift the unit because the cable or cord could disconnect from the unit, causing the unit to drop on the patient.

WARNING

The SpO

2

in the Welch Allyn Spot Vital signs is not intended for use as an apnea monitor.

WARNING

Consider the SpO

2

an early warning device. As a trend toward patient deoxygenation is indicated, use laboratory instruments to analyze blood samples to completely understand the patient’s condition.

Directions for Use

Temperature Warnings

WARNING

Single-use, disposable probe covers, available from Welch Allyn, limit patient cross-contamination. The use of any other probe cover or the failure to use a probe cover may produce temperature errors and is specifically not recommended.

WARNING

Use only oral probes (blue cap) for taking oral and axillary temperatures. Use only rectal probes (red cap) for taking rectal temperatures. The use of the wrong probe may produce temperature errors.

WARNING

Do not allow the tip of the temperature probe to come into contact with any heat source (e.g., hands or fingers) prior to taking a temperature measurement. If this occurs, discard the probe cover and start the temperature determination again.

WARNING

Long-term continuous monitoring beyond three to five minutes is not recommended in any mode.

IR Communications Port Warnings

WARNING

The Welch Allyn Spot Vital Signs contains an infrared communications port for isolated communications with external devices. The port is located on the side of the device to preclude direct eye contact on a continual basis when viewing the display. As a precaution, do not look directly into the infrared port during operation.

General Cautions

A caution statement in this manual identifies a condition or practice, which if not corrected or discontinued immediately, could lead to equipment failure, equipment damage, or data loss.

Caution

If the accuracy of any measurement is in question, check the patient's vital sign(s) by an alternate method, then check to make sure the device is functioning properly.

Caution

Ensure the device is placed on a secure surface or use one of the optional mounting accessories.

Caution

Do not place fluids on the device.

7

8

Welch Allyn Spot Vital Signs

Blood Pressure Cautions

Caution

Extremity and blood pressure cuff motion should be minimized during blood pressure determinations.

Caution

If the blood pressure cuff is not at heart level, the difference in reading due to the hydrostatic effect should be noted. The value of 1.80 mmHg must be added to the displayed reading for every inch (2.5 cm) above heart level. The value of 1.80 mmHg must be subtracted from the displayed reading for every inch (2.5 cm) below heart level.

Caution

Proper blood pressure cuff size and placement is essential to the

accuracy of the blood pressure determination. See “Chart for Determining Blood

Pressure Cuff Size” on page 23 for blood pressure cuff sizing information.

Caution

When measuring blood pressure on children younger than 3 years of age, it is recommended that the Pressure Preset (initial inflation pressure) be set at 160 mmHg or lower.

SpO

2

Cautions

Caution

The pulse oximeter is calibrated to determine the percentage of arterial oxygen saturation of functional hemoglobin. Significant levels of dysfunctional hemoglobin such as carboxyhemoglobin or methemoglobin may affect the accuracy of the measurement.

Caution

Physiological conditions, medical procedures, or external agents that may interfere with the pulse oximeter’s ability to detect and display measurements include dysfunctional hemoglobin, arterial dyes, low perfusion, dark pigment, and externally applied coloring agents such as nail polish, dye, or pigmented cream.

Caution

Some sensors may not be appropriate for a particular patient. If at least

15 seconds of perfusion pulses cannot be observed for a given sensor, change sensor location or sensor type for perfusion to resume.

Caution

When selecting a sensor, consider the patient’s weight and activity level, the adequacy of perfusion, the available sensor sites, the need for sterility, and the anticipated duration of monitoring.

Temperature Cautions

Caution

The Welch Allyn Spot Vital Signs is FDA cleared to measure the axillary temperature in Normal Mode for children under the age of 4. Normal Mode axillary temperatures may not be accurate on older children or adults.

THE

WELCH ALLYN SPOT VITAL SIGNS IS NOT INTENDED TO BE USED ON

NEONATAL PATIENTS.

Directions for Use

Avertissements et précautions de sécurité

Tout le personnel l’utilisant doit être familiarisé avec les informations globales de sécurité contenues dans ce résumé. Ce manuel comprend également des avertissements et précautions spécifiques. Il est possible que ces avertissements et précautions spécifiques ne soient pas indiqués dans ce résumé.

Avertissements généraux

Les avertissements de ce manuel identifient les conditions ou pratiques qui, si elles ne sont pas corrigées ou arrêtées immédiatement, risquent de provoquer des blessures, des maladies ou le décès du patient.

AVERTISSEMENT

Le Welch Allyn Spot Vital Signs est conçu pour être utilisé par des médecins. Si ce manuel présente des techniques de vérification médicale ponctuelle, seul un clinicien formé sachant comment relever et interpréter les signes vitaux d’un patient doit utiliser ce système.

AVERTISSEMENT

Les informations contenues dans ce manuel sont un guide détaillé du fonctionnement du Welch Allyn Spot Vital Signs. Pour obtenir des résultats satisfaisants, merci de lire ce manuel attentivement avant d’essayer d’utiliser l’appareil.

AVERTISSEMENT

Spot Vital Signs n’est pas conçu pour relever des données sur des patients nouveau-nés. Selon la norme AAMI SP10:1992, un nouveau-né est un enfant de moins de 28 jours, s’il est né à terme, (37 semaines de gestation ou plus). Sinon, jusqu’à 44 semaines de gestation.

AVERTISSEMENT

Le Welch Allyn Spot Vital Signs n’est pas protégé en cas de défibrillation.

AVERTISSEMENT

Le Welch Allyn Spot Vital Signs n’est pas conçu pour un monitorage continu. Ne pas laisser l’appareil sans surveillance lors du relevé de mesures sur un patient.

AVERTISSEMENT

Afin d’assurer la sécurité du patient, utiliser uniquement des accessoires et fournitures (à savoir des brassards, des flexibles, des sondes de température, des capteurs de SpO

2

, etc.) recommandés ou fournis avec le Spot

Vital Signs. L’utilisation d’accessoires non-approuvés avec le Spot Vital Signs peut affecter la sécurité du patient et/ou de l’opérateur.

AVERTISSEMENT

Cet appareil n’est pas conçu pour une utilisation en présence d’un mélange anesthésique inflammable avec l’air, l’oxygène ou le protoxyde d’azote. Une explosion pourrait se produire.

AVERTISSEMENT

Éviter de comprimer les tubes du brassard ou le tuyau de tensiomètre de tension artérielle du Welch Allyn Spot Vital Signs. La compression des tubes du brassard ou du tuyau de tensiomètre peut entraîner des erreurs du système au niveau du dispositif.

AVERTISSEMENT

Il convient de procéder avec soin afin d’empêcher l’eau ou tout autre fluide de pénétrer dans les connecteurs du dispositif. Si cela se produit, les connecteurs doivent être séchés à l’air chaud. Toutes les fonctions d’utilisation doivent ensuite être contrôlées.

AVERTISSEMENT

Tout Spot Vital Signs ayant subi une chute ou un dommage doit être vérifié par un technicien qualifié qui s’assurera de son bon fonctionnement avant utilisation. Ne pas utiliser le Welch Allyn Spot Vital Signs en cas de signes d’endommagement. Contacter le Service clientèle de Welch Allyn pour obtenir de l’aide.

9

10

Welch Allyn Spot Vital Signs

AVERTISSEMENT

Tous les trois mois, vérifier que la sonde de température, le câble SpO

2

et les accessoires ne s’effilochent pas et qu’ils ne sont endommagés de quelque façon. Remplacer si nécessaire.

AVERTISSEMENT

Hormis la batterie, aucune pièce de l’appareil n’est remplaçable par l’utilisateur. Retourner le Spot Vital Signs au centre d’entretien autorisé.

AVERTISSEMENT

Le Spot Vital Signs ne doit pas être utilisé sur des patients reliés à des machines cardiaques/pulmonaires.

AVERTISSEMENT

Le Spot Vital Signs ne fonctionne pas efficacement sur des patients souffrant de convulsions ou de tremblements.

AVERTISSEMENT

Ce dispositif se conforme aux normes courantes exigibles en matière de brouillage électromagnétique et ne devrait ni provoquer d'interférences ni en recevoir de la part d'autres équipements. Par mesure de précaution, éviter d’installer l’appareil à proximité d’autres équipements.

AVERTISSEMENT

Ce dispositif n’est pas conçu pour une utilisation manuelle en cours de fonctionnement.

AVERTISSEMENT

Welch Allyn recommande de laisser la batterie dans l’appareil, même si ce dernier n’est pas utilisé pendant de longues périodes. En effet, laisser la batterie dans l’appareil ne présente aucun danger.

AVERTISSEMENT

Ne pas stériliser en autoclave.

AVERTISSEMENT

Welch Allyn n’est pas responsable de l’intégrité de toute installation de montage. Welch Allyn recommande au client de contacter son service d’ingénierie biomédicale ou d’entretien afin de s’assurer de la fiabilité, la sécurité et l’installation professionnelle de tout accessoire de montage.

Avertissements relatifs à la pression artérielle

AVERTISSEMENT

Afin d’assurer la précision et la sécurité de la pression artérielle chez l’enfant, le brassard Welch Allyn pour enfant (5200-03), le brassard longue durée mono-pièce Welch Allyn pour enfant en bas-âge (5082-203-3) et le brassard mono-pièce jetable Welch Allyn pour enfant en bas-âge (5082-93-3) sont les plus petits brassards autorisés pour utilisation sur de jeunes enfants et des nourrissons. La circonférence du bras de l’enfant doit se situer dans la plage indiquée sur le brassard.

AVERTISSEMENT

Les valeurs de pression artérielle peuvent être imprécises si des brassards et/ou flexibles de pression artérielle autres que ceux fournis par

Welch Allyn pour le Spot Vital Signs sont utilisés.

AVERTISSEMENT

Les patients souffrant d’arythmies modérées à aiguës peuvent délivrer des mesures de pression artérielle imprécises.

AVERTISSEMENT

Lorsque plusieurs valeurs de pression artérielle sont relevées sur le même patient, il est recommandé de contrôler régulièrement l’extrémité et le site du brassard de pression artérielle afin de détecter une ischémie, un purpura et/ou une neuropathie éventuels.

AVERTISSEMENT

Ne pas changer le(s) connecteur(s) sur le tuyau du tensiomètre de cet appareil pour un type luer. Les connecteurs de type luer sont couramment utilisés dans des systèmes de perfusion par intraveineuse.

L’utilisation de connecteurs luer sur un tuyau de brassard de pression artérielle crée le risque que le tuyau de pression artérielle soit connecté par erreur à une intraveineuse du patient, entraînant l’introduction d’air dans l’appareil circulatoire du patient.

Directions for Use

11

Avertissements relatifs à SpO

2

AVERTISSEMENT

N’utiliser Spot Vital Signs avec l’option Masimo ou Nellcor

SpO

2

qu’avec les accessoires et capteurs de la marque Masimo ou Nellcor, respectivement. L’utilisation de capteurs ou de câbles erronés ou non-approuvés peut entraîner des performances incorrectes.

AVERTISSEMENT

Les rallonges et capteurs SpO

2

sont conçus pour être utilisés uniquement avec les mesures d’oxymétrie pulsée. Ne pas essayer de connecter ces câbles à un PC ou tout autre appareil similaire.

AVERTISSEMENT

Avant utilisation, lire soigneusement le mode d’emploi du capteur, y compris tous les avertissements, les précautions et instructions.

AVERTISSEMENT

Ne pas utiliser un câble SpO

2

ou de capteur endommagé. Ne pas utiliser un capteur dont les composants optiques sont exposés.

AVERTISSEMENT

Un tissu peut être endommagé par une application ou une durée d’utilisation incorrecte d’un capteur SpO

2

. Inspecter le site du capteur comme indiqué dans le mode d’emploi du capteur.

AVERTISSEMENT

Ne pas utiliser les capteurs en cours d’examen d’imagerie par résonnance magnétique (IRM). Le courant produit peut potentiellement provoquer des brûlures. L’oxymètre de pouls MS board peut affecter l’image de l’IRM et l’appareil d’IRM peut affecter la précision des mesures de l’oxymètre de pouls.

AVERTISSEMENT

Certaines conditions environnementales ambiantes, erreurs d’application de capteur et certaines conditions de patients peuvent affecter les valeurs de SpO

2

et le signal de pouls.

AVERTISSEMENT

Ne pas immerger les câbles patient ou capteur dans de l’eau, des solvants ou des solutions de nettoyage (les capteurs et les connexions ne sont pas étanches). Ne pas utiliser de rayonnement, de vapeur ou d’oxyde d’éthylène pour la stérilisation.

AVERTISSEMENT

Ne pas utiliser le câble SpO

2

ou le câble d’alimentation pour soulever l’unité. En effet, ces deux câbles sont susceptibles de se déconnecter de l’appareil, entraînant la chute de l’appareil sur le patient.

AVERTISSEMENT

Le SpO

2

du Welch Allyn Spot Vital signs n’est pas conçu pour une utilisation comme moniteur d’apnée.

AVERTISSEMENT

Considérer le SpO

2

comme un dispositif d’avertissement précoce. Si une tendance à la désoxygénation du patient est indiquée, utiliser des instruments de laboratoire pour analyser des prélèvements sanguins afin de comprendre complètement l’état du patient.

12

Welch Allyn Spot Vital Signs

Avertissements relatifs à la température

AVERTISSEMENT

Les embouts de sonde jetables à usage unique, disponibles auprès de Welch Allyn, limitent les contaminations entre patients. Il est spécialement déconseillé d’utiliser tout autre embout de sonde ou de ne pas utiliser d’embout. En effet, cela peut générer des erreurs de température.

AVERTISSEMENT

N’utiliser que des sondes orales (bleues) pour le relevé de températures orales et axillaires. N’utiliser que des sondes rectales (rouges) pour le relevé de températures rectales. L’utilisation de la mauvaise sonde peut produire des erreurs de température.

AVERTISSEMENT

Ne pas laisser l’extrémité de la sonde de température entrer en contact avec une source de chaleur (par ex. les mains ou les doigts) avant de procéder à un relevé de température. Si cela se produit, jeter l’embout de la sonde et reprendre la détermination de la température.

AVERTISSEMENT

Un monitorage continu longue durée de trois à cinq minutes n’est pas recommandé, quel que soit le mode.

Avertissements relatifs au port de communication infrarouge

AVERTISSEMENT

Le Welch Allyn Spot Vital Signs contient un port de communication infrarouge pour les communications isolées avec des périphériques externes. Ce port se trouve sur le côté de l’appareil pour empêcher tout contact visuel direct continu lors de la consultation de l’affichage. À titre de précaution, ne pas regarder directement le port infrarouge en cours de fonctionnement.

Précautions générales

Dans ce manuel, Attention identifie les conditions ou pratiques qui, si elles ne sont pas corrigées ou arrêtées immédiatement, risquent de provoquer des pertes de données, un endommagement ou une défaillance du matériel.

Attention

Si la précision de toute mesure est mise en question, vérifier le(s) signe(s) vital (vitaux) du patient en employant une autre méthode, puis s’assurer que l’appareil fonctionne correctement.

Attention

S’assurer que l’appareil est situé sur une surface sûre ou utiliser un des accessoires de montage optionnels.

Attention

Ne pas placer de fluides sur l’appareil.

Directions for Use

Précautions relatives à la pression artérielle

Attention

Veiller à minimiser le mouvement de l’extrémité et du brassard de pression artérielle en cours de détermination de la pression artérielle.

Attention

Si le brassard de tensiomètre n’est pas au niveau du coeur, la différence de valeur due à l’effet hydrostatique doit être notée. La valeur de

1,80 mmHg doit être ajoutée à la valeur affichée pour chaque pouce (2,5 cm) au-dessus du niveau du coeur. La valeur de 1,80 mmHg doit être retirée à la valeur affichée pour chaque pouce (2,5 cm) en dessous du niveau du cœur.

Attention

Il est essentiel que le brassard de tensiomètre soit à la taille et l’emplacement adéquats pour assurer la précision de la détermination de la pression artérielle. Voir “Tableau de détermination de la taille de brassard de tensiomètre” on page 17 pour obtenir des informations sur la taille du brassard de pression artérielle.

Attention

Lors de la mesure de la pression artérielle sur des enfants de moins de 3 ans, il est recommandé de définir le réglage de la pression (pression de gonflage initiale) sur une valeur inférieure ou égale à 160 mmHg.

Précautions relatives à SpO

2

Attention

L’oxymètre de pouls est étalonné pour déterminer le pourcentage de saturation en oxygène du sang artériel de l’hémoglobine fonctionnelle. Des niveaux importants d’hémoglobine dysfonctionnelle comme la carboxyhémoglobine ou méthémoglobine peuvent affecter la précision de la mesure.

Attention

Certaines conditions physiologiques, interventions médicales ou substances externes sont susceptibles d’interférer avec les fonctions de détection et de mesure de l’oxymètre de pouls, par exemple les hémoglobines dysfonctionnelles, les colorants artériels, les conditions de faible perfusion et les pigments foncés, ainsi que les agents de coloration appliqués par voie externe, tels que le vernis à ongle, les teintures ou les crèmes pigmentées.

Attention

Certains capteurs peuvent s’avérer inadéquats pour un patient en particulier. S’il n’est pas possible d’observer au moins 15 secondes d’impulsions de perfusion pour un capteur donné, modifier l’emplacement du capteur ou le type de capteur pour la perfusion afin de reprendre l’opération.

Attention

Lors du choix d’un capteur, prendre en considération le poids du patient et son niveau d’activité, l’adéquation de la perfusion, les sites de capteurs disponibles, le besoin de stérilité et la durée prévue du monitorage.

Précautions relatives à la température

Attention

Le Welch Allyn Spot Vital Signs est approuvé par la FDA pour mesurer la température axillaire en mode normal pour les enfants de moins de

4 ans. Les températures axillaires du mode normal peuvent ne pas être précises sur des enfants plus âgés ou des adultes.

LE WELCH ALLYN SPOT VITAL SIGNS

N’EST PAS CONÇU POUR UNE UTILISATION SUR DES NOUVEAU-NÉS.

13

14

Welch Allyn Spot Vital Signs

2

Controls, Indicators, and Connections

In this section, all drawing and text are representative of the Spot Vital Signs with all available options. Your device may not include all functions, depending on the options purchased.

Unpacking Checklist

Unpack the Welch Allyn Spot Vital Signs and applicable accessories, identify each item with the following checklist and inspect for missing items. Retain the shipping materials in the event of shipping damage or for return, if necessary, to Welch Allyn for repair or warranty service. All Spot Vital Signs include the following components:

Spot Vital Signs Device.

This device automatically measures and displays blood pressure and pulse rate. Options include thermometry and pulse oximetry.

Directions for Use Manual.

Read this manual thoroughly before using Spot Vital Signs.

Save this manual for reference.

Warranty Card.

This card validates the Spot Vital Signs warranty. Fill out the warranty card and mail it today.

Blood Pressure Cuff.

Latex free blood pressure cuff with connectors. Other size cuffs are available separately.

Blood Pressure Hose.

Latex-free pressure hose with connectors to attach various sizes of blood pressure cuffs to the Spot Vital Signs.

AC Power Transformer and Cord Assembly.

Provides power to the Spot Vital Signs and charges the internal battery.

Quick Reference/Error Code Card.

Attach this quick operating and error code guide to the device handle, mobile stand, or wall mount.

Possible Attachments

Spot Vital Signs may include the following items based on the model and accessories purchased:

SureTemp Temperature Probe and Covers.

One oral temperature probe (blue cap) and one box of 25 single-use, disposable probe covers.

Pulse Oximetry (SpO

2

).

The finger clip SpO

2

sensor and extension cable are for use with adult and pediatric patients. Other sensors are available separately.

Note

Report any signs of shipping damage to the carrier. If an item is missing or damaged, contact the Welch Allyn Service Center near you.

15

16

Front Panel Functions

Welch Allyn Spot Vital Signs

Thermometer Eject Button

: push to remove used temperature probe cover.

Pressure Preset Button

: pressing this button allows the user to change the factory inflation default for one reading.

Mode Button:

• holding for 2 seconds while the display is active turns off/on the backlight.

• in Standby Mode, recalls the last patient information.

• with the temperature probe removed from the probe holder, switches the temperature from

Oral to Axillary Mode.

SYS kPa (mmHg)

DIA kPa (mmHg)

SpO

2

%

/ min

Spot Vital Signs

Next Patient/Clear/Cancel Button:

• active display: clears the display.

• in Standby Mode: recalls the last patient information. Pressing a second time clears the screen.

• cancels an active blood pressure measurement and deflates the cuff.

Blood Pressure Start/Stop Button

: initiates a new blood pressure cycle.

Pressing again cancels an active blood pressure measurement and deflates the cuff.

Pressure Hose Connector

: port for blood pressure hose.

Power Button

: controls power to the device.

Directions for Use

LCD (Liquid Crystal Display)

The LCD may indicate any of the following: systolic blood pressure (mmHg or kPa), diastolic blood pressure (mmHg or kPa), temperature (

°

F or

°

C), thermometer mode, pulse rate, pulse signal level, SpO

2

, MAP (mmHg or kPa), and battery charge level.

.

Option no longer available.

SYS mmHg

DIA mmHg

Systolic and Diastolic display:

if MAP is turned on, the screen toggles between the systolic and diastolic values, and the word

“MAP” and the MAP value.

Date/Time

: indicates that the user must set/re-set the current date and time.

Measurement Indicator

displays the blood pressure, SpO2, or temperature icon as Spot

Vital Signs is taking the respective measurement.

:

SpO

2

%

/ min

M

P

SpO

2

Display

: shows the percent saturation of arterial hemoglobin (for devices with SpO

2

only).

Pulse Display

: shows the pulse rate.

Temperature Display and Indicator:

shows the temperature in Fahrenheit or Celsius (for devices with

SureTemp only).

Monitor Mode Temperature

: indicates the thermometer is in Monitor Mode (for devices with SureTemp only).

Out-of-range indicator:

shows the patient’s temperature reading above or below the measurement range limits (for devices with SureTemp only).

Icon not used.

Thermometer Mode icon:

shows temperature mode (for devices with SureTemp only).

Temperature Probe Problem

: indicates a temperature probe problem

(for devices with SureTemp only).

Battery Level indicator

Battery Charging

: indicates the device is powered through the AC power transformer.

: displays the battery charge level.

17

18

Top, Side, and Rear Panel Connections

Welch Allyn Spot Vital Signs

Probe Cover Storage Compartment

: storage space for one box of probe covers.

SpO

2

Cable Connection Port

(for units with SpO

2

only)

Temperature Probe Holder

: storage space for the temperature probe when not in use (for devices with SureTemp only).

Suretemp Thermometer

Connection Port

(for devices with SureTemp only).

Battery Door

IR Data Interface

:

Port for communicating with an external device.

AC Power

Connection Port

Threaded Insert

: to mount the

Spot Vital Signs to a mobile stand.

3

Internal Configuration

You can change several device operating parameters in the Internal Configuration Mode.

When changed, these settings become the default power-up settings. You will also see non-changeable device configurations for technical service purposes.

To enter the Internal Configuration Mode:

1.

Turn the Spot Vital Signs off.

2.

Press and hold the

Power

and

Blood Pressure Start/Stop

buttons. The device enters the Internal Configuration Mode and displays the software version.

3.

Press the

Mode

button to cycle through the Internal Configuration menu until you see the menu option displayed on the screen.

4.

Use the

Next Patient/Clear/Cancel

or

Blood Pressure Start/Stop

buttons to change the default setting.

5.

Press the

Mode

button once to save the change and press the

Power

button to exit the Internal Configuration Mode.

Table 2. Configuration Menu Options

Setting Description

Blood Pressure Calibration

Displays “Cal”

Prepares the Spot Vital Signs for calibration. Only qualified personnel should verify the

Spot Vital Signs blood pressure calibration. For more details, see “Checking the Blood

Pressure Calibration” on page 26.

Inflation Pressure Preset Level

Displays “PrP”

120, 140, 160, 180, 200, 240, 280 mmHg. Factory default is 160 mmHg.

On or off. Disables or enables the front panel Pressure Preset button.

Pressure Preset Level

Displays “PrP“

Backlight

Displays “BLT”

Mean Arterial Pressure

Displays “MAP”

Date/Time

On or off.

On or off.

Temperature Scale

Displays “TMP MOD”

Blood Pressure Units

Displays “BP”

Battery Readings

Displays “BAT”

Battery Life

Displays “LFE”

Changes or updates the actual date and time.

Fahrenheit (°F) or Celsius (°C) Normal Mode / Fahrenheit (°F) or Celsius (°C) Monitor

Mode mmHg or kPa.

Displays the total battery voltage.

Total number unit measurements. Displayed information only; operator cannot change.

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20

Internal Configuration Welch Allyn Spot Vital Signs

4

Setup

Blood Pressure Hose and Cuff Connections

Have available the Spot Vital Signs, blood pressure cuff, and blood pressure hose.

1.

Inspect the pressure hose; note that one end has a connector fitting and the other end does not. Attach the end without the connector fitting to the pressure hose

connector (see page 16). Verify that the pressure hose is completely inserted over the

connector and that the fit is snug.

2.

Join the other end of the pressure hose to the blood pressure cuff pneumatic tubing.

Twist the connectors together until finger-tight.

DO NOT OVERTIGHTEN

.

Temperature Probe Connection

The Welch Allyn Spot Vital Signs is available with two probes — one for oral/axillary temperatures (blue cap), and one for rectal temperatures (red cap). The rectal probe is an accessory item that is ordered separately.

Press down on the tab on top of the connector and insert the connector into the temperature probe connector port on the back of the Spot Vital Signs. The probe connector only fits into Spot Vital Signs one way. Verify the connector clicks into place.

Insert the temperature probe into the probe holder on the top of the Spot Vital Signs.

To remove the temperature probe, press down on the connector tab and lift out.

SpO

2

Sensor Connection

Spot Vital Signs is available with a wide variety of SpO

2

sensors and ships with a reusable finger sensor and extension cable. All other sensors are accessory items that are sold separately.

1.

Align the shape and pin configuration of the extension cable connector to the SpO

2 cable connection port on the top side of the Spot Vital Signs device.

2.

Push the connector firmly into the SpO

2

cable connection port.

3.

Align the opposite end of the extension cable to the sensor cable connector and firmly push them together.

Note

Use only Masimo or Nellcor SpO

2

sensors and accessories with the Spot Vital

Signs with Masimo or Nellcor configurations, respectively.

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22

Welch Allyn Spot Vital Signs

Quick Reference/Error Code Card

The Quick Reference/Error Code Card should be attached either to the Spot Vital Signs handle, the Mobile Stand, or the Wall Mount.

AC Power Connection

Use the Spot Vital Signs with AC or battery power (after charging the battery).

1.

Insert the round transformer connector into the AC power connection port on the left

of the Spot Vital Signs (see page 18).

2.

Insert the line cord into the line connector on the transformer then plug the power cord on the transformer into the AC main power source to charge the battery.

Charging the Battery

CHARGE THE BATTERY FOR SIXTEEN (16) HOURS PRIOR TO INITIAL USE

.

Attach the AC power transformer to the Spot Vital Signs then plug the transformer into the AC main power source.

While charging, the charger icon remains on and the battery icon segments continuously sequence. When the battery is fully charged, all battery icon segments display.

As the battery voltage level drops the segments turn off from left to right. If the Spot Vital

Signs is not plugged in to charge when the second last segment is turned off the Spot

Vital Signs issues a warning beep. As the voltage level drops to compromise measurements an error beep is heard and all other display fields turn off. Spot Vital Signs beeps at increasingly frequent intervals until it finally powers itself off.

If not used for extended periods of time then recharge the battery.

Standby Mode

When the device is powered up, but has not been used for 2 minutes, it goes into

Standby Mode. “Z Z Z” appears across the top of the display with no backlight. Standby

Mode conserves battery power.

To bring the Spot Vital Signs out of Standby Mode, press the

Mode

or

Pressure Preset

button or begin a patient measurement.

5

Blood Pressure

Caution

When measuring blood pressure on children younger than age 3, it is recommended that the Pressure Preset (initial inflation pressure) be set at 160 mmHg or lower.

Selecting the Blood Pressure Cuff

Note

A durable blood pressure cuff is included with your Spot Vital Signs. A full range of blood pressure cuff sizes are available as accessory items.

Careful sizing of the blood pressure cuff is important to the accuracy of blood pressure readings. If the blood pressure cuff is too small, you may have false high readings. If the blood pressure cuff is too large, you may have false low readings. Please refer to the range markings on the blood pressure cuff for correct blood pressure cuff sizing. When there is an area of overlap whereby you could use a smaller or larger blood pressure cuff, it is strongly recommended that you use the larger size blood pressure cuff.

Determining Blood Pressure Cuff Size with the Markings

Wrap the blood pressure cuff around the patient’s upper arm and visually check it. The blood pressure cuff is marked with a distinct white edge and two divisions that indicate

“range.” When the blood pressure cuff is properly fit, the edge meets the blood pressure cuff at some point within the range.

Chart for Determining Blood Pressure Cuff Size

You can also determine blood pressure cuff size by measuring the patient’s arm circumference midway between the elbow and shoulder, then use the chart below to select the correct blood pressure cuff.

Cuff Size

Child

Adult

Large Adult

Thigh

Reusable Two-Piece Cuff

(1 per pack)

5200-03

5200-01

5200-02

5200-10

Maximum Range

(cm)

20.8

31.5

38.4

47.4

Maximum Range

(in)

8.2

12.4

15.1

18.7

23

24

Welch Allyn Spot Vital Signs

Durable

One-Piece Cuff

(Single Unit)

5082-203-3

5082-204-3

5082-205-3

5082-206-3

5082-207-3

5082-208-3

Disposable

One-Piece Cuffs

(5 pack)

5082-93-3

5082-94-3

5082-95-3

5082-96-3

5082-97-3

5082-98-3

Cuff Size

Small Child

Child

Small Adult

Adult

Large Adult

Thigh

Minimum

(cm)

Maximum

(cm)

Minimum

(inches)

Maximum

(inches)

12.4

15.8

20.0

25.3

32.1

40.7

16.8

21.3

27.0

34.3

43.4

55.0

4.9

6.2

7.9

10.0

12.6

16.0

6.6

8.4

10.6

13.5

17.1

21.7

THE WELCH ALLYN SPOT VITAL SIGNS IS NOT INTENDED FOR USE ON NEONATAL

PATIENTS

.

To ensure pediatric blood pressure accuracy and safety, the Welch Allyn Child Print Cuff

(5200-03), the Welch Allyn Small Child Durable One-Piece Cuff (5082-203-3), and the

Welch Allyn Small Child Disposable One-Piece Cuff (5082-93-3) are the smallest cuffs allowed for use with young children and infants. The circumference of the child’s arm must fit within the range markings on the blood pressure cuff.

To position the blood pressure cuff:

The preferred blood pressure measurement site for adults and children is the upper arm.

Keep the patient’s arm relaxed and motion-free during measurement(s).

WARNING

Do not place the blood pressure cuff on any extremity that is used for intravenous infusions or any area where circulation is compromised.

WARNING

Do not change the connector(s) on the blood pressure cuff tubing of this device to luer type. Luer type connectors are commonly used in intravenous infusion systems. Using the luer connectors on blood pressure cuff tubing creates the risk that the blood pressure tubing could be mistakenly connected to a patient's intravenous line, resulting in the introduction of air into the patient's circulatory system.

Note

Blood pressure cuff inflation during an SpO

2

measurement may cause inaccurate

SpO

2

results when used on the same extremity.

Wrap the blood pressure cuff snugly with room between the blood pressure cuff and the arm for no more than two fingers. Excessive tightness may cause venous congestion and discoloration of the limb. Possible error may occur if the blood pressure cuff is wrapped too loosely, preventing proper inflation.

Place the blood pressure cuff on a bare arm; clothing interferes with measurement accuracy. Verify that the cuff artery marker is placed over the brachial artery. Ensure that the hose is not twisted, kinked, or compressed, as this may cause measurement errors.

Directions for Use

25

To set the pressure preset level (one time only):

1.

Press and hold the

Pressure Preset

button for half a second. Spot Vital Signs displays

“PrP” (pressure preset) in the SYS and the inflation pressure in the DIA displays, respectively.

2.

Push the

Pressure Preset

button. The blood pressure cuff inflation pressure decreases in 20 mmHg increments beginning at 160 mmHg (160 -> 140, 120, 200,

180, 160).

To return to the normal operating mode, push the

Next Patient/Clear/Cancel

button or wait 3 seconds.

The inflation pressure resets to the default pressure setting after completing one blood pressure cycle. The factory default is 160 mmHg.

There is a disable feature in the Internal Configuration Mode that allows the facility to

disable this button, see page 19.

To initiate a blood pressure measurement:

1.

Ensure that the blood pressure cuff is properly sized and wrapped around the patient’s upper arm (or alternate site, as necessary).

2.

With the device powered on, press the

Blood Pressure Start/Stop

button.The Spot Vital Signs inflates the blood pressure cuff to the appropriate pressure and displays the pressure as the blood pressure measurement is in process.

Pressing the

Blood Pressure Start/Stop

or the

Next Patient/Clear/Cancel

button at any time during a blood pressure determination cancels the measurement and rapidly deflates the blood pressure cuff.

When the measurement cycle is complete the Spot Vital Signs beeps once and displays the systolic, diastolic, and pulse rate* measurements for two minutes

(unless another measurement is active). If the MAP is turned on then the Spot Vital

Signs toggles between the blood pressure reading and the MAP value.

If Spot Vital Signs cannot take a successful blood pressure measurement it beeps twice and displays a “C” error code unless the measurement was purposely stopped.

* Pulse rate, as determined from the blood pressure measurement method, is displayed with the blood pressure reading only if the SpO

2

option is not in use. If the SpO

2

function is in use, all pulse rate determinations are a result of the SpO

2

measurement method.

Reviewing Information from the Last Cycle

The Spot Vital Signs holds the last patient measurement cycle in memory. The information is held in memory until the unit is turned off or you initiate the next patient’s measurement. If the display is blank, press the

Mode

button to review data from the last measurement cycle.

26

Welch Allyn Spot Vital Signs

Checking the Blood Pressure Calibration

The Welch Allyn Spot Vital Signs is manufactured to the highest industry standards for quality and accuracy. The device is manufactured using calibrated pressure standards traceable to NIST (National Institute of Standards and Technology). Welch Allyn recommends that blood pressure calibration for the Spot Vital Signs is checked on an annual basis using the following procedure.

Put the Spot Vital Signs into its blood pressure calibration check mode. In this mode, the device continuously displays the measured pressure and closes the pressure release valve.

1.

Enter the internal configuration mode (see “Internal Configuration” on page 19).

2.

Press the

Blood Pressure Start/Stop

button to close the device’s internal valve to apply an external pressure.

3.

Connect the Spot Vital Signs as shown to a calibrated pressure meter (verify certificate is traceable to the National

Institute of Standards and Technology.

The

Spot Vital Signs

pressure meter testing the Spot Vital

Signs must have an accuracy of better than ±3 mmHg.

Use a fixed volume or a blood pressure cuff wrapped around a cylinder for the stabilization volume.

MODE

C

4.

Pressurize the Spot Vital Signs to slightly above 250 mmHg. Bleed the pressure to approximately 250 mmHg. Clamp and record the pressure reading and the

Stabilization

Volume

(150 - 500cc)

Calibrated Pressure

Meter (traceable to

NIST)

Pressure Source measurement standard. Repeat this step for 150 and 50 mmHg (approximate).

5.

Calculate the difference between the readings. Subtract the rated accuracy of the pressure measurement standard from the ±3 mmHg rated accuracy of Spot Vital

Signs. This is the

pass/fail criteria

to determine if the device is within calibration or not. If the differences between Spot Vital Signs and the pressure measurement standard are within the pass/fail criteria at all specified pressures, then the device is within calibration.

If the Spot Vital Signs needs re-calibration the procedures are included in the Spot Vital

Signs Service Manual. Alternatively, send the device back to Welch Allyn for calibration by contacting Technical Service.

Note

The pass/fail criteria for the blood pressure calibration check depends upon the accuracy of the pressure measurement standard used. For example:

If the pressure measurement standard used is rated with an accuracy of ±0.1 mmHg, the pass/fail criteria is ±2.9 mmHg in order to guarantee that the instrument under test is within ±3 mmHg of NIST.

If the pressure measurement standard used is rated with an accuracy of ±1.0 mmHg, the pass/fail criteria is ±2.0 mmHg in order to guarantee that the instrument under test is within ±3 mmHg of NIST.

Welch Allyn recommends using a pressure meter that is as accurate as possible when performing calibration checks. Welch Allyn offers two different pressure measurement standards for use:

Directions for Use

27

Setra Pressure Meter, calibrated accuracy of ±0.1 mmHg (part no. 2270-01)

Netech Pressure Meter, calibrated accuracy of ±1.0 mmHg (part no. 200-2000IN)

Use of other pressure measurement standards is acceptable, provided they have an accuracy of better than ±3 mmHg, are traceable to NIST, and have a current calibration.

Note

Do not take more than 3 minutes to take the readings, as the Spot Vital Signs will open its pressure relief valve as a safety feature. If this occurs, turn the device off and start over.

The Spot Vital Signs has the option to measure pressure in kPa units. If the device is set to kPa instead of mmHg, temporarily set the device to mmHg units or convert all pressures to kPa units.

28

Welch Allyn Spot Vital Signs

6

Temperature

WARNING

Long-term continuous monitoring beyond three to five minutes is not recommended in any mode.

Selecting Temperature Operation Mode

When configured with the temperature option, the Welch Allyn Spot Vital Signs takes a temperature in either Normal or Monitor Mode.

In the Normal Mode, the thermometer “predicts” body temperature in approximately 4 seconds for oral temperatures, 10 seconds for axillary temperatures, and 15 seconds for rectal temperatures.

Monitor Mode is normally used when difficult situations prevent taking an accurate temperature in the Normal Mode. In Monitor Mode, maintain probe contact with the tissue for at least 3 minutes for accurate oral/rectal temperature measurement, and 5 minutes for accurate axillary temperature measurement.

The default setting for the Spot Vital Signs thermometer is Normal Mode.

Temperature Measurement Range Indicators

The following display appears when temperatures are outside of the measurement range of the device:

Condition Temperature

Temperature is outside of high measurement range of the device

Temperature is outside of low measurement range of the device

Fahrenheit

Celsius

Fahrenheit

Celsius

Display

109.4°

43°

86°

30°

Audible

Notification

No

No

Normal Mode

Patient actions may interfere with accurate oral temperature readings. Ingesting hot or cold liquids, eating food, chewing gum or mints, brushing teeth, smoking, or performing strenuous activity may affect oral temperature readings for up to 20 minutes after activity has ended.

29

30

Welch Allyn Spot Vital Signs

Probe contact with electrodes or bandages, poor tissue contact, taking an axillary temperature over clothing, or prolonged exposure of axilla to ambient air can cause inaccurate axillary temperature readings.

WARNING

To ensure optimal accuracy, always confirm that the correct mode is selected.

WARNING

Use only Welch Allyn probe covers. Using other manufacturers’ probe covers or no probe cover may produce temperature measurement errors and/or inaccuracy.

To take a temperature in oral or axillary mode:

WARNING

Do not take an axillary temperature over the patient’s clothing. Direct contact between the patient’s skin and the probe is required.

Caution

Use the temperature probe with the blue cap to obtain accurate oral or axillary temperatures.

Note

Normal Mode axillary temperatures are FDA cleared for children under the age of four. THE WELCH ALLYN SPOT VITAL SIGNS IS NOT INTENDED FOR USE ON

NEONATAL PATIENTS.

1.

Verify that the correct probe (blue cap) is installed.

2.

Hold the probe handle with your thumb and two fingers on the sides of the probe handle and withdraw the probe.

3.

Verify the desired temperature mode is in the temperature display area and the desired temperature mode icon is flashing.

If the desired mode is not selected, press the

Mode

button until the LCD displays

“OrL” or “ALy”.

4.

Insert the probe into a probe cover and press the probe handle down firmly. The probe handle moves slightly to engage the probe cover.

5.

Quickly put the probe in place.

a.

For oral temperatures, place the probe tip under the patient’s tongue on either side of the mouth to reach the sublingual pocket and ask the patient to close his/ her lips.

SUBLINGUAL POCKET

SUBLINGUAL POCKET

Directions for Use

31

b.

For axillary temperatures, lift the patient’s arm so that the entire axilla is easily seen and place the probe as high as possible in the axilla. Do not allow the probe tip to come into contact with the patient until the probe is placed in the measurement site. Any prior contact between the probe tip and the tissue with another material may cause inaccurate readings. Verify that axillary tissue completely surrounds the probe tip and place the arm snugly at the patient’s side.

6.

Firmly hold the probe in place and keep the tip of the probe in contact with the tissue throughout the measurement process. During the measurement process, the temperature display area displays rotating “walking” segments.

Spot Vital Signs beeps once after reaching the final temperature. The temperature display area displays the patient temperature. Spot Vital Signs displays the current temperature for two minutes after the probe is placed back in the holder. The display then goes blank (unless another measurement is active).

If Spot Vital Signs displays a probe position icon during the temperature determination, the temperature display alternates between the final predicted temperature and the letter “P”.

To switch to Monitor Mode, leave the probe in place after obtaining a reading and press the

Mode

button once. The temperature display shows an “M” to indicate

Monitor Mode. Once in Monitor Mode proceed to Step 5 on page 33.

7.

Remove the probe after the temperature measurement is complete and firmly press the ejection button on the top of the probe to release the probe cover.

8.

Return the probe to Spot Vital Signs.

To take a temperature in Rectal Mode:

WARNING

Incorrect insertion of probe can cause bowel perforation.

WARNING

Washing hands greatly reduces the risk of cross-contamination and nosocomial infection.

Caution

To obtain accurate rectal temperatures, use the temperature probe with the red ejection button.

1.

Verify that the rectal probe (red cap) is installed. Spot Vital Signs only operates in

Rectal Mode if the red rectal probe is installed.

2.

Hold the probe handle with your thumb and two fingers on the sides of the probe handle and withdraw the probe from Spot Vital Signs.

3.

Verify the Spot Vital Signs temperature display shows “rEC” to indicate a rectal probe is in use.

4.

Insert the probe into a probe cover and press the probe handle down firmly. The probe handle moves slightly to engage the probe cover.

5.

Separate the patient’s buttocks with one hand. Use the other hand to gently insert the probe only 5/8 in. (1.5 cm) inside the rectum (less for infants and children). The use of a lubricant is optional.

6.

Tilt the probe so that the tip is in contact with tissue. Continue to separate the buttocks and hold the probe in place throughout the measurement process. During the measurement process, the temperature display area displays rotating “walking” segments.

32

Welch Allyn Spot Vital Signs

Spot Vital Signs beeps once after reaching the final temperature. The temperature display area displays the patient temperature. Spot Vital Signs displays the current temperature for two minutes after the probe is placed back in the holder. The display then goes blank (unless another measurement is active).

If Spot Vital Signs displays a probe position icon during the temperature determination, the temperature display alternates between the final predicted temperature and the letter “P”.

To switch to Monitor Mode after obtaining a reading, leave the probe in place after obtaining a reading and press the Mode button once. The temperature display shows an “M” to indicate Monitor Mode. Once in Monitor Mode proceed to Step 5 on page 33.

7.

Remove the probe after the temperature measurement is complete and firmly press the ejection button on the top of the probe to release the probe cover.

8.

Return the probe to Spot Vital Signs and wash your hands.

Directions for Use

33

Monitor Mode

Monitor Mode displays the temperature of the probe as long as the probe remains in place at the measurement site and remains within the operating patient temperature range. The patient’s temperature will reach final equilibrium in approximately three minutes in the oral and rectal sites and five minutes in the axillary site.

WARNING

Long-term continuous monitoring beyond three to five minutes is not recommended in any mode.

Note

To switch to Monitor Mode without taking a predictive temperature, remove the probe from the holder, attach a new probe cover, and wait one minute. Do not place the probe in the patient’s mouth, underarm, or rectum. After one minute, the thermometer switches to Monitor Mode and an “M” shows in the temperature display. Continue to take the patient’s temperature.

To take a temperature in Monitor Mode:

1.

Verify that the correct probe (oral/axillary = blue cap or rectal = red cap) is installed.

2.

Hold the probe handle with your thumb and two fingers on the sides of the probe handle and withdraw the probe from Spot Vital Signs.

3.

Insert the probe into a probe cover and press the probe handle down firmly. The probe handle moves slightly to engage the probe cover.

4.

Take the patient’s temperature using the Normal Mode as previously described. Leave the probe in place after Spot Vital Signs beeps once and displays the temperature.

Press the

Mode

button once. An “M” appears on the display to indicate Monitor

Mode.

5.

Hold the thermometer in place for a total of three minutes for oral and rectal mode or five minutes for axillary mode. The thermometer will not beep to indicate a final temperature.

6.

Record the temperature before removing the probe from the site; the monitored temperature does not remain on the display once the probe is removed from the site and is not stored in memory for recall.

7.

Remove the probe from the patient and firmly press the ejection button on the top of the probe to release the probe cover.

8.

Return the probe to the Spot Vital Signs to reset the thermometer to Normal Mode.

34

Welch Allyn Spot Vital Signs

7

Pulse Oximetry (Sp0

2

)

Factors that may degrade the performance of the pulse oximeter:

• Excessive ambient light

• Anemia or low hemoglobin concentrations

• Moisture in the sensor

• Incorrect sensor for patient

• Venous pulsations

• Sensor not at heart level • Excessive motion

• Fingernail polish (if finger sensor is used)

• Arterial catheters, blood pressure, and infusion lines, etc.

• Cardiovascular dyes • Improperly attached sensor

• Electrosurgical interference • Poor patient perfusion

WARNING

Tissue damage can be caused by incorrect application or duration of use of an SpO

2

sensor. Inspect the sensor site as directed in the sensor

Directions for Use.

WARNING

Do not use a damaged sensor or pulse oximetry cable or a sensor with exposed optical components.

To take an SpO

2

measurement:

If blood pressure measurement is occurring simultaneously, place the finger sensor on the limb opposite the one with the blood pressure cuff.

1.

Insert the patient’s finger completely into the sensor; the thumb is specifically not recommended for use with the finger clip sensor.

The pulse signal bar graph illuminates, indicating the patient’s pulse at the sensor site.

The sensor takes approximately 10 seconds to determine the initial SpO

2

% value and pulse rate. When the initial values are determined, they are shown in the SpO

2 display and the pulse rate display, respectively. If the accuracy of any measurement does not seem reasonable, first use an alternate means to check the patient’s vital signs and then check the Spot Vital Signs for proper functioning.

Spot Vital Signs measures a patient’s SpO

2

for up to 10 minutes. After 10 minutes,

Spot Vital Signs displays a C9 error code and beeps twice. This error code means that the use has exceeded the 10-minute time limit.To clear the error code, disconnect the sensor from Spot Vital Signs and then re-attach it or press the

Next Patient/Clear/

Cancel

button.

2.

Check sensor sites periodically to assess circulation, sensor positioning, and skin sensitivity.

3.

Remove the sensor from the patient. The device continues to display the last SpO

2 reading.

35

36

Welch Allyn Spot Vital Signs

8

Error Indications and Interpretation

The following table of conditions and error codes provides a quick reference of the descriptions and probable causes of error codes.

To clear the error code:

Power the Spot Vital Signs off, wait five seconds, and power on. If the error code reappears then power the Spot Vital Signs off and disconnect the battery for five minutes.

Reconnect the battery and power on. If the error code continues to reappear, call Welch

Allyn for a Service Notification Number (see “Technical Assistance” on page 56).

Press the Blood Pressure Start/Stop button to reset flashing patient alarm conditions.

Error Codes

Table 1. General

Code

E11

C12

Description

Internal safety violation

Ambient temperature out of range

C13 Battery failure

E0.0 - E9.9

Temperature module malfunction

E42 Internal communications error

E20 - E50 General internal malfunction

Corrective Action

Check patient, contact Technical Service.

Adjust ambient temperature or device location.

Use wall transformer.

Contact Technical Service.

Disconnect the battery and wait 5 minutes.

Reconnect the battery and then set the date and time,

see “Blood Pressure Hose and Cuff Connections” on page 21.

Contact Technical Service.

Table 2. Blood Pressure

Code

C02

C03

Description

Auto-zero failure

Inflation too rapid

C04

C05

C06

E10

Excessive inflation time

Excessive noise

Measurement was outside of device’s measurement range

Blood pressure cuff overpressure condition

Corrective Action

Check for air obstruction, limit patient movement.

Check for kinked blood pressure cuff tubing, pressure hose, or other air obstruction.

Check for air leaks.

Check patient condition, blood pressure cuff placement, limit patient movement.

Check patient condition.

Check patient condition.

37

38

Welch Allyn Spot Vital Signs

Table 3. Temperature

Code

C20

Description

Broken/missing probe

P Loss of tissue contact

E0.2, E0.3

Ambient temperature out of range

C22 10-minute diagnostic time exceeded

Code

E7

C6

C8

C9

Table 4. SpO

2

Description

Internal SpO

2

error.

SpO

2

pulse rate out of range

Faulty SpO

2

sensor.

SpO

2

time limit exceeded.

Corrective Action

Replace probe.

Ensure proper probe positioning.

Adjust ambient temperature or device location.

Remove probe, discard probe cover, retake temperature.

Corrective Action

Retake reading.

Check patient condition.

Replace sensor.

Remove sensor from patient. Reapply sensor and retake reading.

Directions for Use

Causes and Corrective Action

Table 5. Inaccurate Blood Pressure Readings

Possible Cause

Incorrect blood pressure cuff size.

Use Welch Allyn approved blood pressure cuffs only.

Patient’s arm position

Arm movement during blood pressure cycle

Blood pressure taken over clothing

Arrhythmia

Explanation and Corrective Action

Determine correct blood pressure cuff size.

• Use reference markings on blood pressure cuff.

• Measure patient’s arm circumference midway between elbow and shoulder (see

“Chart for Determining Blood Pressure Cuff Size” on page 23 to select correct

blood pressure cuff size).

Ensure patient’s arm is at heart level.

Keep arm still during blood pressure cycle.

• Movement may cause inaccuracies from artifact.

Take blood pressure on a bare arm.

Check for regularity of heart rate (palpate pulse or check device).

• Moderate to severe heart rate irregularities may make blood pressure difficult to measure.

Incorrect reference Use the correct Korotkoff sound to determine diastolic blood pressure.

• Many listeners incorrectly equate diastolic blood pressure with the disappearance of sound only (phase 5). The Welch Allyn Spot Vital Signs was developed using the American Heart Association recommendations, which state that phase 5 be used unless sound continues to 0 mmHg, in which case the change in the quality of sound (phase 4) is to be used.

Deflate blood pressure cuff no faster than 3 mmHg per second.

• One of the major sources of error in auscultatory blood pressure measurement is deflating the blood pressure cuff too quickly. The American Heart Association recommends deflation no faster than 3 mmHg per second.

Only use a sphygmomanometer that is calibrated.

• An uncalibrated sphygmomanometer may take inaccurate blood pressure measurements.

Check blood pressure immediately prior to Welch Allyn Spot Vital Signs reading.

Change in blood pressure between auscultatory reading and Welch Allyn Spot Vital

Signs reading

Poor auscultatory sound recognition by observer

Use higher quality stethoscope. Have a different observer check patient’s blood pressure.

Note: Differences of up to 10 mmHg are considered normal and occur for a number of reasons including intra-patient blood pressure variability, observer hearing differences, and auscultatory deflation rate.

Table 6. Cuff Inflation and Deflation with No Blood Pressure Reading Displayed (or Error Code in

Display)

Possible Cause

Leak in pneumatic system

Arm movement during cycle

Blood pressure cuff tubing or pressure hose movement artifact

Explanation and Corrective Action

Ensure all blood pressure cuff attachments are tight. Carefully check for leaks in the blood pressure cuff, tubing, and pressure hose attached to the device.

Keep arm still during blood pressure cycle. Movement may cause inaccuracies from artifact.

Do not contact blood pressure cuff tubing or pressure hose during blood pressure cycle. Movement may cause inaccuracies from artifact.

39

40

Welch Allyn Spot Vital Signs

Table 7. No Blood Pressure Cuff Inflation

Possible Cause

Connections between device and blood pressure cuff loose

Explanation and Corrective Action

Check all connections (do not overtighten).

Table 8. Temperature Malfunction

Possible Cause

Error code displayed

Explanation

Broken probe

Low temperature readings

Improper probe placement

No temperature displayed Probe not replaced

Corrective Action

Replace probe. Consult Service Manual. Notify biomedical department or Welch Allyn Technical Support.

Place probe in most posterior sublingual pocket when in

Oral Mode. Verify patient has had nothing to eat or drink for 20 minutes.

Replace probe in holder prior to taking another temperature.

Table 9. SpO

2

Malfunction

Possible Cause Corrective Action

Sensor in place but no SpO

2 display

on Insert the patient’s finger completely into sensor.

Verify blood pressure and SpO

2

measurements are not taken on the same extremity.

Verify the sensor cable is correctly plugged into device.

Verify you are using the correct sensor. Use only Masimo or Nellcor SpO

2

sensors and accessories with the Welch Allyn Spot Vital Signs with Masimo or Nellcor configurations, respectively.

Table 10. Device Does Not Turn On

Possible Cause

Low battery

Device not powering up

Explanation and Corrective Action

Check connections between device and transformer, and transformer and wall receptacle.

Unplug unit from wall receptacle and check for breaks in cord. If connections are secure, check electrical outlet.

Charging indicator is on if connections are good and the device is plugged into a working outlet.

Notify biomedical department or Welch Allyn Technical Support.

Table 11. Blood Pressure Cuff Too Tight (Over Inflation)

Possible Cause

Pressure preset too high

Explanation and Corrective Action

Check default Pressure Preset setting in internal configuration mode. Unless patient has underlying systolic hypertension, set pressure preset at 160 mmHg. (If systolic blood pressure greater than pressure preset, the device automatically increases an additional 40 mmHg.)

Directions for Use

Table 12. Blood Pressure Cuff Pops Off

Possible Cause

Inappropriate blood pressure cuff size

Blood pressure cuff applied inside out

Explanation and Corrective Action

Determine blood pressure cuff size with the blood pressure cuff markings or see

“Chart for Determining Blood Pressure Cuff Size” on page 23. If blood pressure cuff

continues to pop off, notify biomedical department or Welch Allyn Technical Support.

Re-apply blood pressure cuff. Make sure Welch Allyn label is facing away from arm.

Table 13. Blood Pressure Cuff Deflating Too Slowly

Possible Cause

Normal operation

Pressure preset too high

Patient movement

Small leak in pneumatic system

Explanation and Corrective Action

Typical time to take a reading is 20 to 45 seconds; 165 seconds is the maximum.

Check default pressure preset setting in internal configuration mode.

Have patient sit still. Do not have arm tight against chest wall, as respiration may affect speed and accuracy of blood pressure measurement.

Check blood pressure cuff tubing and pressure hose for leaks.

41

42

Welch Allyn Spot Vital Signs

9

Specifications

Patient Population

The Welch Allyn Spot Vital Signs is designed for use with adult and pediatric patients.

Welch Allyn defines a pediatric patient as 29 days or more of age.

THE WELCH ALLYN SPOT VITAL SIGNS IS NOT INTENDED FOR USE ON NEONATES

.

Welch Allyn defines neonates as children 28 days or less of age, born at term (37 weeks gestation or more), otherwise up to 44 gestational weeks.

Blood Pressure

Cuff Pressure Range

Cuff Inflation Factory

Default

Systolic Range

Diastolic Range

Accuracy

Determination Time

Pulse Rate Range

Pulse Rate Accuracy

Overpressure Cutoff

0 mmHg to 300 mmHg

160 mmHg

60 mmHg to 250 mmHg

30 mmHg to 160 mmHg

Blood pressure accuracy meets or exceeds SP10-1992 AAMI standards for non-invasive blood pressure accuracy (AAMI standard: ± 5 mmHg mean error,

8 mmHg standard deviation). Blood pressure accuracy is validated for pressure measurement using the upper arm only.

Typical: 20 to 45 seconds

Maximum: 165 seconds

40 bpm to 200 bpm

±5.0%

305 mmHg -0/+15 mmHg

Temperature

Accuracy

Range

Determination Time

Calibration accuracy: + 0.2° F (+ 0.1° C).

Maximum: 109.4° F/43.0° C

Minimum:

86.0° F/30.0° C

Oral: approximately 4 seconds

Axillary: approximately 10 seconds

Rectal: approximately 15 seconds

43

44

Welch Allyn Spot Vital Signs

Pulse Oximetry

Masimo Sensor Accuracy Guide

Accuracy specified when used with Masimo SET pulse oximetry monitors or with licensed Masimo SET pulse oximetry modules using Masimo patient cables, during no motion. Numbers present ± 1 standard deviation. Plus or minus one standard deviation represents 68% of the population. SpO

2

accuracy from 70% to 100%. Pulse rate accuracy from 25 to 240 bpm.

Performance Measurement Range

Perfusion

SpO

2

Accuracy

Pulse Rate Accuracy

SpO

2

: 70 to 100%

Pulse Rate: 25 - 240 beats per minute (BPM)

0.02% to 20%

Saturation: 70% to 100%

No Motion: Adults, Pediatrics ± 2 digits

Motion: Adults, Pediatrics ± 3 digits

Low Perfusion: Adults, Pediatrics ± 2 digits

Pulse Rate: 25 to 240 bpm

No Motion: Adults and Pediatrics ± 3 digits

Motion: Adults and Pediatrics ± 5 digits

Low Perfusion: Adults and Pediatrics ± 3 digits

Table 14. Masimo Sensor Accuracy Guide

Sensor

LNCS-DCI

LNCS-DCIP

LNCS-ADTX

LNCS-PDTX

LNCS INF-L

LNOP-DCI

LNOP-DCIP

LNOP-ADT

LNOP-PDT

LNOP INF-L

Weight Range

> 30 kg

10 to 50 kg

> 30 kg

10 to 50 kg

3 to 20 kg

> 30 kg

10 to 50 kg

> 30 kg

10 to 50 kg

3 to 20 kg

Saturation Accuracy

No Motion

± 2%

± 2%

± 2%

± 2%

± 2%

± 2%

± 2%

± 2%

± 2%

± 2%

Motion

± 3%

± 3%

± 3%

± 3%

± 3%

± 3%

± 3%

± 3%

± 3%

± 3%

Pulse Rate Accuracy

No Motion

± 3 bpm

± 3 bpm

± 3 bpm

± 3 bpm

± 3 bpm

± 3 bpm

± 3 bpm

± 3 bpm

± 3 bpm

± 3 bpm

Motion

± 5 bpm

± 5 bpm

± 5 bpm

± 5 bpm

± 5 bpm

± 5 bpm

± 5 bpm

± 5 bpm

± 5 bpm

± 5 bpm

Masimo Patents

The Masimo sensors and cables are covered under one or more of the following U.S.A. patents: 5,758,644; 5,823,950; 6,011,986; 6,157,850; 6,263,222; 6,501,975; and other applicable patents listed at www.masimo.com/patents.htm.

Directions for Use

45

Nellcor

®

Sensor Accuracy Guide

Accuracy specifications are based on controlled hypoxia studies with healthy, non-smoking adult volunteers over the specified saturation SpO

2 range. Pulse oximeter

SpO

2

readings were compared to SaO

2 values of drawn blood samples measured by hemoximetry. All accuracies are expressed as + “X” digits. This variation equals plus one standard deviation (+ 1 SD), which encompasses 68% of the population.

Pulse Rate Range

Pulse Rate Accuracy

25 to 240 bpm

±3 bpm

±3 bpm (low perfusion)

Table 15. OxiMax Sensor Models, Single Patient Use

Sensor Models

MAX-AI

MAX-PI

MAX-II

MAX-RI

1

1

The accuracy specification has been determined between saturations of 80% to 100%.

SpO

2

Range

70% to 100%

± 2

± 2

± 2

± 3.5

Table 16. OxiCliq Sensor Models, Single Patient Use

Sensor Models

OXICLIQ-PI

SpO

2

Range

70% to 100%

± 2.5

Table 17. Reusable Sensor Models

Sensor Models

D-YS (Infant to Adult)

D-YS and D-YSE

D-YS and D-YSPD

DS-100A

OXI-A/N (Adult)

OXI-P/I (Pediatric/infant)

SpO

2

Range

70% to 100%

± 3

± 3.5

± 3.5

± 3

Adult: ± 3

± 3

Nellcor Patents

Covered by one or more of the following US Patents: 4,802,486; 4,869,254; 4,928,692;

4,934,372; 5,078,136; 5,351,685; 5,485,847; 5,533,507; 5,577,500; 5,803,910; 5,853,364;

5,865,736; 6,083,172; 6,708,049; Re. 35,122 and foreign equivalents.

46

Welch Allyn Spot Vital Signs

Mechanical

Dimensions

Weight

Mounting

Height: 9.7 inches (24.6 cm)

Length: 5.7 inches (14.5 cm)

Depth: 4.7 inches (12.0 cm)

Approximately 4.6 pounds (2.2 kg)

Self-supporting on rubber feet

Custom Mobile Stand

Custom Wall Mount

Custom IV Pole Mount

May be hand-carried when held by the rear handle.

Portability

Electrical

Power Requirements

Battery

Patient-rated isolation transformer is connected to AC mains:

North American Version:120VAC, 60Hz. 0.13A Input, 7.2VDC, 1.0A Output

International Version:240VAC, 50Hz 0.065A Input, 7.2VDC, 1.0A Output

Australian Version:240VAC, 50Hz, 13VA Input, 7.2VDC, 1.0A Output

Lead acid, with external charger.

A fully charged battery supports 130 typical blood pressure determinations taken at

7-minute intervals. The battery is 90-100% charged after 12 hours of charging. The battery automatically charges when the Spot Vital Signs is powered through the AC power transformer. The battery charges faster when the instrument is not in operation.

Environmental

Operating Temperature

Storage Temperature

Transport Temperature

Relative Humidity

Operating Altitude

+10

°

to +40

°

C (Thermometer operating temperature 16° to 40° C)

+50

°

to +104

°

F (Thermometer operating temperature 61° to 104° F)

-20

°

to +50

°

C

-4

°

to +122

°

F

-20

°

to +49

°

C

-4

°

to +122

°

F

15 to 90% (non-condensing)

-170 to +4877 m

-557 to +16,000 ft.

Directions for Use

Guidance and Manufacturer’s Declaration

Emissions and Immunity Information

Electromagnetic Emissions

The 420 Series Spot Vital Signs is intended for use in the electromagnetic environment specified below. The customer or user of the 420 Series

Spot Vital Signs should assure that it is used in such an environment.

Emissions Test

RF emissions

CISPR 11

RF emissions

CISPR 11

Harmonic emissions

IEC 61000-3-2

Voltage fluctuations/ flicker emissions

IEC 61000-3-3

Compliance

Group 1

Class B

Class A

Complies

Electromagnetic Environment - Guidance

The 420 Series Spot Vital Signs uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

The 420 Series Spot Vital Signs is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

47

48

Welch Allyn Spot Vital Signs

Electromagnetic Immunity

The 420 Series Spot Vital Signs is intended for use in the electromagnetic environment specified below. The customer or user of the 420 Series

Spot Vital Signs should assure that it is used in such an environment.

Immunity Test IEC 60601

Test Level

± 6 kV contact Electrostatic discharge

(ESD)

± 8 kV air

IEC 61000-4-2

Electrical fast transient/ burst

±2 kV for power supply lines

Compliance Level

± 6 kV contact

± 8 kV air

±2 kV for power supply lines

Electromagnetic Environment - Guidance

Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

Mains power quality should be that of a typical commercial or hospital environment.

IEC 61000-4-4

Surge

IEC 61000-4-5

Voltage dips, short interruptions, and voltage variations on power supply input lines.

IEC 61000-4-11

Power frequency

(50/60Hz) magnetic field

IEC 61000-4-8

±1 kV for input/output lines

±1 kV differential mode

±1 kV for input/output lines

±1 kV differential mode Mains power quality should be that of a typical commercial or hospital environment.

±2 kV common mode

>95% dip in 0.5 cycle

±2 kV common mode

>95% dip in 0.5 cycle

60% dip in 5 cycles

30% dip for 25 cycles

60% dip in 5 cycles

30% dip for 25 cycles

Mains power quality should be that of a typical commercial or hospital environment. If the user of the 420 Series Spot Vital

Signs requires continued operation during power mains interruptions, it is recommended that the 420 Series Spot Vital

Signs be powered from an uninterruptible power supply or battery.

>95% dip in 5 seconds

3 A/m

>95% dip in 5 seconds

3 A/m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

Directions for Use

49

Electromagnetic Immunity

The 420 Series Spot Vital Signs is intended for use in the electromagnetic environment specified below. The customer or user of the 420 Series

Spot Vital Signs should assure that it is used in such an environment.

Immunity Test IEC 60601

Test Level

Conducted RF

IEC 61000-4-6

Radiated RF

IEC 61000-4-3

3 Vrms

150 kHz to 80 MHz

3 V/m

80 MHz to 2.5 GHz

Compliance

Level

Electromagnetic Environment - Guidance

Portable and mobile RF communications equipment should be used no closer to any part of the 420 Series Spot Vital Signs including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.

Recommended separation distance

V1 = 3 Vrms

d

= (1.17)

P

E1 = 3 V/m

d

= (1.17)

P

80 MHz to 800 MHz

d

= (2.33)

P

800 MHz to 2.5 GHz where

P

is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and

d

is the recommended separation distance in metres (m).

Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, a

should be less than the compliance level in each frequency range.

b

Interference may occur in the vicinity of equipment marked with the following symbol:

Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.

Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.

a

Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio,

AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the 420

Series Spot Vital Signs is used exceeds the applicable RF compliance level above, the 420 Series Spot Vital Signs should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the 420 Series

Spot Vital Signs.

b

Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

50

Welch Allyn Spot Vital Signs

Recommended Separation Distances Between Portable and Mobile RF Communications Equipment and the 420 Series Spot

Vital Signs

The 420 Series Spot Vital Signs is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or user of the 420 Series Spot Vital Signs can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the 420 Series Spot Vital Signs as recommended below, according to the maximum output power of the communications equipment.

Rated Max. Output

Power of Transmitter

(W)

0.01

0.1

1

10

100

Separation Distance According to Frequency of Transmitter (m)

150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz

d

= (1.17)

P

0.11667

0.36894

1.1667

3.6894

11.667

d

= (1.17)

0.11667

0.36894

1.1667

3.6894

11.667

P

d

= (2.33)

0.23333

0.73785

2.3333

7.3785

23.333

P

For transmitters rated at a maximum output power not listed above, the recommended separation distance

d

in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where

P

is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.

Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.

Directions for Use

Patents

D392,043 and other patents pending.

Agency Approvals

CERTIFIED TO: CAN/CSA STD C22.2 NO. 601.1

CONFORMS TO: IEC 60601, UL STD 60601-1

Welch Allyn PTY, Ltd - Australia

Metro Centre

Unit 5/38 South Street

Rydalmere NSW 2116, Australia

EMC Framework of Australia

The CE mark on this product indicates that it has been tested to and conforms with the provisions noted within the 93/42/

EEC Medical Device Directive.

EC REP

Authorized European Representative Address:

European Regulatory Manager

Welch Allyn Ltd.

Navan Business Park

Dublin Road

Navan, County Meath, Republic of Ireland

Tel.: +353 46 90 67700 • Fax: +353 46 90 67756

51

52

Welch Allyn Spot Vital Signs

10

Maintenance

Welch Allyn will make available,upon request, circuit diagrams and other information which will assist appropriately qualified technical personnel in repair of this device. Please

reference “4200-89E” on page 61.

Cleaning

Spot Vital Signs

Caution

Do not use ethyl alcohol to clean the Spot Vital Signs device.

Caution

Do not sterilize or autoclave the Spot Vital Signs.

Occasionally wipe the Spot Vital Signs, as necessary, with a cloth slightly dampened with appropriately diluted, non-staining disinfectant solution. Use either 70% isopropyl alcohol,

10% chlorine bleach solution, or mild detergent in warm water. Never immerse the Spot

Vital Signs in any type of fluid.

Note

Prevent water or other fluids from entering any connectors. Should this occur, dry the connectors with warm air. Check all measurement functions for proper operation.

Blood Pressure Cuff

Caution

Do not press with a hot iron.

Clean the blood pressure cuff with a damp cloth, or wash in water with soap or detergent.

Before washing the blood pressure cuff, remove the tube fitting(s), close off tubes with plugs (available as accessory 5082-163) and place the hook and loop fasteners in the closed position. After washing, allow the blood pressure cuff to air dry. Re-assemble the tube fitting(s).

Disinfection

: You may use glutaraldehyde-type liquid disinfectants on the durable blood pressure cuff. Prolonged use of these disinfectants at full strength may cause discoloration of the white blood pressure cuff markings.

Sterilization:

Do not use steam or heat to sterilize the blood pressure cuff or pressure hose. If necessary, use gas sterilization.

53

54

Welch Allyn Spot Vital Signs

Cables and Pressure Hose

Wipe the cabling and pressure hose with a damp cloth moistened in a mild detergent solution. Do not immerse.

Temperature Probe

Periodically wipe the temperature probe clean with an alcohol-dampened cloth, warm water, or properly diluted, non-staining disinfectant. Do not immerse the probe.

SpO

2

Sensor

WARNING

Do not immerse the sensor in water, solvents, or cleaning solutions

(the sensors and connections are not waterproof). Do not use irradiation, steam, or ethylene oxide for sterilization.

Clean the reusable SpO

2

sensor with a 70% isopropyl alcohol solution and allow to air dry.

Do not immerse the sensor or cable.

Every 3 months, inspect the temperature probe, SpO

2

cord, and accessories for fraying or other damage. Replace as necessary.

Battery Removal and Replacement

Caution

Only use the Welch Allyn 4200-84 lead acid battery. Using the incorrect battery will cause damage to the Spot Vital Signs and void the warranty.

As necessary, replace the internal battery after heavy use or the battery no longer charges. Use a battery with the same part number.

1.

Turn the Spot Vital signs off and disconnect the AC power transformer cord.

2.

Remove the 4 screws holding the battery door using a phillips-head screwdriver.

Remove the battery door to expose the battery.

3.

Tip the Spot Vital Signs to slide the battery out. Disconnect and discard the old battery per local regulations. Reconnect the new battery as shown as quickly as possible to prevent loss of power to the unit and subsequent loss of clock time.

Battery

Connector

Directions for Use

4.

Slide the new battery completely into the compartment. Lay the connector on the battery. The relief pocket in the battery door purposely provides sufficient clearance for the battery connector .

55

Relief Pocket

Battery

Battery Connector

5.

Replace the battery door and tighten each of the 4 screws.

6.

Connect the AC power transformer to the Spot Vital Signs and charge the new battery for 16 hours. It is possible to use the Spot Vital Signs during this charging period.

The battery is a lead-acid battery. In the USA, call 1-800-SAV-LEAD for instructions on how to recycle. For users outside the US please contact your local authorities on recycling.

Masimo SpO

2

Calibration Check

Use a Masimo-approved SpO

2

simulator (Fluke Biotek Index 2 or Clinical Dynamics

SmartSat) to check the SpO

2

accuracy. There is no way to change the calibration of the

SpO

2

module. If the SpO

2

is out of calibration, contact Technical Service.

Nellcor SpO

2

Functional Check

Use a Nellcor SpO

2

simulator (SRC-MAX ) to check the SpO

2

functionality. There is no way to change the functionality of the SpO

2

module. If the SpO

2

is not functioning properly, contact Technical Service.

SpO

2

Accessory Disposal

Dispose of all finger sensors and cables in accordance with facility, local, and goverment regulations.

Temperature Calibration Check

Use the 9600 Plus Calibration Tester to check the SureTemp thermometer accuracy. If the thermometer is out of calibration, contact Technical Service.

56

Welch Allyn Spot Vital Signs

Service Manual/Spare Parts

A Service Manual is available upon request to qualified electronic personnel. The Service

Manual is a comprehensive guide to troubleshooting, service, and repair of the Spot Vital

Signs.

Also included with the Service Manual is a complete spare parts list. Order spare parts

from your local Welch Allyn Service Center listed on page ii.

Service Loaners

Service loaners are provided, on request, when a Welch Allyn Service Center provides service. Loaners for products repaired while under the original warranty, or while under extended warranty or service contract, are provided free of charge and are shipped within

48 hours of notification of need. Welch Allyn pays the shipment charges.

For service repairs outside of warranty or contract, loaners are available for a nominal daily charge and shipment. This is subject to availability. Loaners are shipped pre-paid; however, this charge is added to the service charges.

Service Policy

A Welch Allyn Service Center must approve and perform all repairs on products under warranty.

Unauthorized repairs will void the warranty

. Qualified electronics personnel or a

Welch Allyn service center should repair products out of warranty.

Technical Assistance

If you have an equipment problem that you cannot resolve, call the Welch Allyn Service

Center nearest you during normal business days at the phone numbers listed on page ii.

If you are advised to return a product to Welch Allyn for repair or routine maintenance, schedule the repair with the service center nearest you.

Before returning a product for repair, you must obtain authorization from Welch

Allyn. Our service personel will give you a Service Notification number. Note this number on the outside of your shipping box. Service centers will not accept returns without a Service Notification number for delivery.

11

Supplies and Accessories

Latex-Free Blood Pressure

Table 1. Cuff and Bag Combination

Catalog #

5200-01

5200-02

Description

Cuff and bladder, adult, one tube

Cuff and bladder, large adult, one tube

Table 2. One-Piece Cuff

Durable Cuff

Catalog #

5082-203-3

5082-204-3

5082-205-3

5082-206-3

5082-207-3

5082-208-3

Description

One-piece cuff, small child, one tube

One-piece cuff, child, one tube

One-piece cuff, small adult, one tube

One-piece cuff, adult, one tube

One-piece cuff, large adult, one tube

One-piece cuff, thigh adult, one tube

Table 3. Replacement Cuffs and Bladders

Catalog #

5200-04

5200-05

5200-06

5200-11

Description

Adult Bladder, one tube

Large Adult Bladder, one tube

Child Bladder, one tube

Thigh Bladder, one tube

Table 4. Miscellaneous Blood Pressure Accessories

Catalog #

5200-12

5200-19

Description

Straight Pressure Hose (8ft./2.4M)

Straight Pressure Hose (5ft./1.5M)

Catalog #

5200-10

5200-03

Description

Cuff and bladder, thigh, one tube

Cuff and bladder, child, one tube

Disposable Cuff

Catalog #

5082-93-3

Description

One-piece cuff, small child, one tube (box of 5)

5082-94-3

5082-95-3

5082-96-3

5082-97-3

5082-98-3

One-piece cuff, child, one tube (box of 5)

One-piece cuff, small adult, one tube (box of 5)

One-piece cuff, adult, one tube (box of 5)

One-piece cuff, large adult, one tube (box of 5)

One-piece cuff, thigh, one tube (box of 5)

Catalog #

5082-01

5082-16

5082-18

5082-64

Description

Adult cuff (sleeve)

Large adult cuff (sleeve)

Child cuff (sleeve)

Thigh cuff (sleeve)

Catalog #

5200-08

Description

Calibration T-Connector

57

58

Pulse Oximetry Accessories and Supplies

Masimo

Table 5. Adhesive Sensors: Single-Patient Use

Catalog # Description

LNCS-ADTX Adhesive Finger Sensor - Adult (20 per case)

LNCS-PDTX Adhesive Finger Sensor - Pediatric (20 per case)

LNCS INF-L Adhesive Finger Sensor - Infant (20 per case)

LNOP-ADT

LNOP-PDT

Adhesive Adult sensor (20 per case)

Adhesive Pediatric sensor (20 per case)

LNOP INF-L Adhesive Infant sensor (20 per case)

Weight Range

>30 kg

10 to 50 kg

3 to 20 kg

>66 lbs (30 kg)

22 to 110 lbs

(10 to 50 kg)

3 to 20 kg

Table 6. Reusable Sensor

Catalog # Description

LNCS-DCI Finger sensor - adult

LNCS-DCIP Finger sensor - pediatric

LNOP-DCI Finger sensor - adult

LNOP-DCIP Finger sensor - pediatric

Welch Allyn Spot Vital Signs

Weight Range

>66 lbs (30 kg)

10 to 50 kg

>66 lbs (30 kg)

10 to 50 kg

Quantity

1

1

1

1

Table 7. Sensor Cables

Catalog #

LNC-4-WA

Description

4-foot cable with DB-9 connector for LNCS

LNC-10-WA 10-foot cable with DB-9 connector for LNCS

PC-04-WA 4-foot cable with DB-9 connector for LNOP

PC-08-WA 8-foot cable with DB-9 connector for LNOP

Weight Range

NA

NA

NA

NA

Quantity

1

1

1

1

Directions for Use

Nellcor

Table 8. OxiMax Adhesive Sensors: Single-patient use

Catalog #

MAX-AI

MAX-PI

MAX-II

MAX-RI

SRC-MAX

Description

Adult sensor

Pediatric sensor

Infant sensor

Adult nasal sensor

Portable oximetry tester

Weight Range

>30 kg

10 - 50 kg

3-20 kg

>50 kg

Quantity

24

24

24

24

59

Table 9. OxiMax OxiCliq® Sensors: Reusable cable

Catalog #

OC-3

OXICLIQ PI

Description

OxiCliq sensor cable (3 ft)

Pediatric oxygen transducer, user with OC-3 cable

Weight Range

10 - 50 kg

Quantity

1

Case of 24

Table 10. OxiMax Reusable Sensors

Catalog #

DS-100A

OXI-A/N

OXI-P/I

D-YS

D-YSE

D-YSPD

Description

Durasensor

®

adult oxygen transducer

Oxiband

®

OXI-A/N, adult/neonatal* transducer

Oxiband OXI-P/I, pediatric/infant transducer

Dura-Y

®

oxygen transducer

Ear clip (use with Dura-Y sensor)

PediCheck™ pediatric spot-check sensor (use with

Dura-Y sensor)

Weight Range Quantity

>40 kg 1

<3 kg or >40 kg 1 sensor/50 wraps

3 - 40 kg

>1 kg

>30 kg

3 - 40 kg

1 sensor/50 wraps

1 sensor/40 wraps

1

1

Table 11. OxiMax Sensor Cables

Catalog #

DEC-4

DEC-8

Description

SpO

2

extension cable, 4 ft.

SpO

2

extension cable, 8 ft.

Quantity

1

1

* The Welch Allyn Spot Vital Signs is not intended for use on neonatal patients.

60

Welch Allyn Spot Vital Signs

Temperature

Table 12. Accessories and Supplies

Catalog #

02678-100

02679-100

05031-101

Description

Oral/axillary probe (9ft./2.7M)

Rectal probe (9ft./2.7M)

Disposable probe covers (1,000 covers, 25/box)

Mounting

Table 13. Accessories and Supplies

Catalog #

4200-60

4200-62

Description

Mobile Stand

Wall Mount

Extended Warranty

Table 14. One-year extended warranty

Catalog #

4200-00B

4200-OTB

4200-N0B

Description

Model 4200B

Model 420TB

Model 42N0B

Catalog #

05031-110

06137-000

01802-110

Description

Disposable probe covers (10,000 covers, 25/box)

Temperature Calibration Key

Model 9600 Plus Calibration Tester

Catalog #

4200-64

4200-70

Description

IV Pole Mount

Anti-Theft Kit

Catalog #

4200-M0B

4200-NTB

4200-MTB

Description

Model 42M0B

Model 42NTB

Model 42MTB

Directions for Use

61

Miscellaneous

Table 15. Accessories and Supplies

Catalog #

4200-84

4200-87X*

4200-88X*

4200-155

4200-89E

4200-100

4200-170

53600

53600B

Description

Lead Acid Battery

Directions for Use

Quick Reference/Error Code Card

Inservice CD (English only)

Service Manual (English only)

Carrying Case

Connectivity Accessory Kit

Printer paper (24 rolls)

Printer paper (4 rolls)

Catalog #

5200-101A

5200-103A

5200-103Z

76400

76402

76404

76406

4200-250

4200-350

Description

AC Power Transformer (US/Canada/Japan)-120V,

60Hz

AC Power Transformer (Europe/UK) -240V, 50Hz

AC Power Transformer (Australia) - 240V, 50Hz

Line Cord (US/Canada/Japan)

Line Cord (Europe)

Line Cord (UK)

Line Cord (Australia)

Pediatric accessory kit (small child, child, small adult cuffs and Nellcor SpO

2

sensor)

Pediatric accessory kit (small child, child, small adult cuffs and Masimo SpO

2

sensor)

* Replace the “X” with the following letter abbreviation to order the appropriate language manual.

Table 16. Printed Material Language List

F

FI

C

DK

Language

Abbreviation

Language

E English

Chinese

Dansk

Français

Suomi

I

N

NL

Language

Abbreviation

Language

G Deutsch

Italiano

Norsk

Nederlands

Language

Abbreviation

Language

PO Polish

P

S

SW

Português

Español

Svensk

62

Welch Allyn Spot Vital Signs

Warranty

Spot

Welch Allyn warrants Spot Vital Signs, when new, to be free of defects in material and workmanship and to perform in accordance with manufacturer's specifications for a period of two years from the date of purchase from Welch Allyn or its authorized distributors or agents. The battery is covered by a one-year warranty against original defects in material or workmanship. Welch Allyn will either repair or replace any components found to be defective or at variance from manufacturer's specifications within this time at no cost to the customer. It shall be the purchaser's responsibility to return Spot Vital Signs to Welch Allyn or an authorized distributor, agent, or service representative. This warranty does not include breakage or failure due to tampering, misuse, neglect, accidents, modification, or shipping. This warranty is also void if the instrument is not used in accordance with manufacturer's recommendations or if repaired by other than Welch Allyn or an authorized agent. Purchase date determines warranty requirements. No other express warranty is given.

Remember to submit the instrument registration/warranty card for warranty validation.

Complete the information and mail the pre-addressed card to Welch Allyn.

Accessories

The Masimo finger sensor and cable are covered by a six-month warranty against original defects in material or workmanship.

The Nellcor DS-100A is covered by a one-year warranty and the Nellcor DEC-4 cable is covered by a three-month warranty against original defects in material or workmanship.

The Reusable Two-Piece Blood Pressure Cuff is covered by a two-year warranty against original defects in material or workmanship.

The SureTemp probe is covered by a one-year warranty against original defects in material and workmanship. Probe covers are intended for single-use only.

63

64

Warranty Welch Allyn Spot Vital Signs

Reorder No. 4200-87E

Material No. 706272 Ver. C

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