IRT10

Wireless Tympanic

Thermometer

Contents

1. General Safety Information ................................................5

1.1 Warnings / Cautions ............................................................................................. 5

2. Introduction ........................................................................6

2.1 Features of the IRT10 Wireless Themometer ................................................ 6

2.2 Intended Use .................................................................................................. 7

2.2 Contraindications ........................................................................................... 7

2.4 About This Manual ......................................................................................... 7

3. Description of Controls, Indicators, Symbols and

3.5 Thermometer Controls and Display .............................................................. 8

3.2 Description of Symbols / Indicators ................................................................ 9

4. Setup ...................................................................................11

4.1 Unpacking and Inspection .............................................................................. 11

4.2 List of Components ........................................................................................ 11

4.3 Connecting the Thermometer to the host ...................................................... 11

4.4 Installing the Batteries .................................................................................... 12

4.5 Pairing the Thermometer and Main Unit ........................................................ 12

5. Using the Thermometer .....................................................13

5.1 Temperature Measurement ............................................................................ 13

6. Care & Cleaning..................................................................15

6.1 General .......................................................................................................... 15

6.2 Returning the IRT10 Thermometer and System Components ....................... 15

6.3 Service ........................................................................................................... 15

6.4 Periodic Safety Checks .................................................................................. 15

7. Troubleshooting ..................................................................16

7.1 General .......................................................................................................... 16

7.2 Obtaining Technical Assistance ..................................................................... 16

8. Electromagnetic Compatibility ..........................................17

9. Speci fi cations .....................................................................21

9.1 Equipment Classi fi cation ............................................................................... 21

9.2 Standards ....................................................................................................... 21

9.3 General .......................................................................................................... 21

9.4 Environmental ................................................................................................ 22

9.5 Measurement Parameters ............................................................................. 22

10. Warranty & Service ..........................................................23

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Notice

This document contains proprietary information that is protected by copyright. All Rights

Reserved. Reproduction, adaptation, or translation without prior written permission is prohibited, except as allowed under the copyright laws.

Warranty

The information contained in this document is subject to change without notice.

Huntleigh Healthcare Ltd makes no warranty of any kind with regard to this material, including, but not limited to, the implied warranties or merchantability and fi tness for a particular purpose.

Huntleigh Healthcare Ltd shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this material.

Revision History

The documentation part number and revision number indicate its current edition. The revision number changes when a new edition is printed in accordance with the revision history of the documentation. Minor corrections and updates which are incorporated at reprint do not cause the revision number to change. The document part number changes when extensive technical changes are incorporated.

© Huntleigh Healthcare Ltd

All rights reserved

The IRT10 is in conformity with the Medical Devices Directive 93/42/EEC as amended by 2007/47/EC and has been subject to the conformity assurance procedures laid down by the Council Directive.

4

Manufactured in the UK by Huntleigh Healthcare Ltd.

As part of the ongoing development programme the company reserves the right to modify speci

fi

cations and materials without notice.

Smartsigns

®

and Huntleigh are registered trademarks of Huntleigh Technology

Ltd.

© Huntleigh Healthcare Ltd. 2017

1. General Safety Information

This section contains important safety information related to general use of the IRT10 wireless thermometer. Other important safety information appears throughout the manual

Important! Before using this equipment, please study this manual carefully and familiarise yourself with the controls, display features and operating techniques.

Ensure each user fully understands the safety and operation of the unit, as misuse may cause damage to the unit or injury to the user or patient.

1.1 Warnings / Cautions

General warning / caution Refer to Instructions for Use

WARNING: Check the equipment prior to use and ensure its safe and proper use.

WARNING: Before use, carefully read directions for use, including all warnings, cautions, and instructions.

WARNING: If the battery shows any signs of damage, leakage, or cracking, it must be replaced immediately, by a quali fi ed service person, and only with a battery approved by the manufacturer.

WARNING: The monitor is intended only as an adjunct in patient assessment. It must be used in conjunction with clinical signs and symptoms.

WARNING: It is possible that any radio frequency transmitting equipment and other sources of electrical noise such as cellular phones, due to close proximity or strength of a source, may result in disruption of performance.

CAUTION: U.S. Federal law restricts this device to sale by or on the order of a licensed healthcare practitioner.

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2. Introduction

WARNING: The Wireless Tympanic Thermometer is intended only as an adjunct in patient assessment. It must be used in conjunction with clinical signs and symptoms.

This manual contains information about the Wireless Tympanic Thermometer (Order code: IRT10).

It is available as an option for the SC300 SPOT CHECK Vital Signs Monitor.

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2.1 Features of the IRT10 Wireless Themometer

Physical

The IRT10 wireless tympanic thermometer is a clinical grade hand held thermometer indicated for the intermittent measurment of body temperature in patients of all ages.

Electrical

The Thermometer is powered by two AAA dry cells.

Display

The Thermometer presents the following information on the integrated display:

• Lens cover indicator

• Wireless pairing status scale ° F

2.2 Intended Use

The Thermometer is intended for use by trained healthcare professionals in healthcare settings to measure human body temperature in patients of all ages.

It uses an infra red technique to measure the amount of infrared energy re fl ected from the tympanic membrane.

2.2 Contraindications

The Thermometer should not be used if the following situations are present:

Do not use the thermometer if there is any blood or drainage in the ear canal.

Do not use the thermometer if the patient presents with in fl amatory condition of the ear canal.

Do not use the thermometer if the ear canal is blocked with cerumen.

Do not use the thermometer if ear drops or medication has been applied to the ear

2.4 About This Manual

Read the entire manual including the Safety Information section, before you operate the monitor.

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8

3. Description of Controls, Indicators,

Symbols and Displays

3.5 Thermometer Controls and Display

1

2

4

3

5

6

3

4

5

6

1

2

Temperature probe status indicator

Start measurment

Display

Infra red sensor

Lens ejector

Battery compartment

Key Function / Display

Battery status

Lens fi lter status

Wireless status

Scale ºC or ºF

Measurement

3.2 Description of Symbols/ Indicators

The symbols and Indicators are described as follows:

Symbols Description

Attention, consult accompanying documents.

Battery charging indicator lamp

Refer to instructions for use

IPX1 Protection against vertically falling water drops

Date of manufacture

SN

Serial number

9

10

Symbols Description

Conformité Européenne Complies with medical device directive 93/42/

EEC

Disposal instructions

Manufacturer

This way Up

Fragile – Handle with care

Limit of stacking layers

Keep dry

4. Setup

WARNING: The IRT10 Wireless Thermometer is a prescription device and is to be operated by quali fi ed personnel only. It is designed for use by medical clinicians.

WARNING: Discarded battery may explode during incineration. Follow local government ordinances and recycle instructions regarding disposal or recycling of device components, including batteries. Do not dispose of batteries in refuse containers.

4.1 Unpacking and Inspection

The Thermometer is shipped in one carton. Examine the carton carefully for evidence of damage. Contact Huntleigh Healthcare Ltd Service Department immediately if any damage is discovered. Return all packing material and Thermometer. Refer to the

Maintenance section for instructions on returning damaged items.

4.2 List of Components

Quantity

1

2

Item

Thermometer

AAA dry cells

1

1

Quantity Item

Lens covers

Cradle

4.3 Connecting the Thermometer to the host

To facilite ease of use, the Thermometer can be fi tted to the SC300 using the cradle supplied.

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4.4 Installing the Batteries

WARNING: Dispose of Battery in accordance with local requirements and regulation. Follow local instructions regarding disposal or recycling of batteries.

CAUTION: Measured or displayed data may not be assured in the low battery or the critical low battery condition.

CAUTION: Discarded battery may explode during incineration. Recycle used batteries properly. Do not dispose of batteries in refuse containers.

Remove the battery cover to expose the battery compartment

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Place new batteries into compartment paying attention to the polarity, close the compartment ensuring it snaps into place.

The system is ready for use

4.5 Pairing the Thermometer and Main Unit

1. Make sure the main unit and ear thermometer are both switched OFF.

2. Press and hold the “ejector key” on the thermometer and switch it ON.

3. The thermometer display will alternate between ºC and ºF and then display “SE”.

4. When “SE” is displayed, release the ejector button and switch the main unit ON.

5. Pairing will be established when the

6. If pariring has failed, no

icon is displayed on the host unit.

icon will be displayed.

5. Using the Thermometer

The Thermometer must be calibrated at least once every two years, contact your service personnel when calibration is necessary

Use only speci fi ed protective lens covers

The protective lens cover is single-use. Repeated use might give rise to cross infection.

The protective lens cover must be used when measuring, if not, it might cause cross infection or inaccurate readings.

Before use, check whether the cover is free from damage, if not, don’t use.

Handle the thermometer with care, it should be stored in the cradle when not in use.

Discard the protective lens cover in accordance with the local regulations.

During the monitoring process, the temperature measuring instrument will automatically check itself once per hour. Self-checking will last 2 seconds, and will not affect the normal working of the temperature monitor.

Measurments are sent via a wireless connection established between the thermometer and the main unit.

Both items (Thermometer and unit) must be paired to enable data transfer.

5.1 Temperature Measurement

1. Install a new protective lens cover to the thermometer.

icon changes to .

3. Position the patient with their head moved to one side, gently pull the ear backward to straighten the ear canal. Gently place the sensor into the ear canal.

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4. Press the START button once, the sensor will sound a quick double beep indicating that its ready to measure.

Press the START button once again and after a short period, the sensor will sound a long single tone indicating that the measurement is complete.

5. Remove the thermometer.

6. The measurement will be shown on the thermometer’s screen, it will be automatically transferred to the monitor.

Thermometer display

Monitor display

7. Press the eject key to remove the disposable lens cover.

8. Place the lens cover in the appropriate waste collection point and place the thermometer onto the unit

6. Care & Cleaning

6.1 General

The probe tip is the most delicate part of the thermometer. It has to be clean and intact to ensure accurate readings.

Gently wipe the surface of the probe tip with a cotton swab or soft cloth moistened with alcohol.

After the alcohol has completely dried, fi t a new lens fi lter and take a temperature measurement.

If the probe tip is damaged, please contact your service agent.

Use a soft, dry cloth to clean the thermometer display and exterior.

Do not use abrasive cleaners.

Never submerge the thermometer in water or any other liquid.

Store thermometer and lens fi lters in a dry location free from dust and contamination and away from direct sunlight.

6.2 Returning the IRT10 Thermometer and

Components

Contact Huntleigh Healthcare Ltd Service Department for shipping instructions. Pack the accessory items in its original shipping carton. If the original carton is not available, use a suitable carton with appropriate packing material to protect the device during shipping.

Return by any shipping method that provides proof of delivery.

6.3 Service

Apart from a 2 year calibration check, the Wireless Thermometer requires no routine service other than cleaning or battery maintenance that is mandated by the user’s institution. For more information, refer to Smartsigns ® Compact 300 service manual.

Quali fi ed service personnel in the user’s institution should perform periodic inspections of the equipment. If service is necessary, contact quali fi ed service personnel or Huntleigh

Healthcare Ltd Service Department.

If the institution’s service personnel cannot correct problems, the equipment should be returned to Huntleigh Healthcare Ltd for service. Contact Huntleigh Healthcare Ltd Service

Department for return instructions.

6.4 Periodic Safety Checks

It is recommended that the following checks be performed every 24 months.

• Inspect the equipment for mechanical and functional damage.

• Inspect the safety relevant labels for legibility.

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7. Troubleshooting

WARNING: If you are uncertain about the accuracy of any measurement, check the patient’s vital signs by alternate means; then make sure the monitor is functioning correctly.

WARNING: Only quali fi ed service personnel should remove the cover.

There are no user-serviceable parts inside.

7.1 General

If the equipment is unable to perform any of its monitoring functions because of the loss of software control or a detected hardware malfunction, an error code is presented.

In the unlikely event of the unit developing a fault, fault codes will be shown in the corresponding area and the related parameters will fl ash on the screen

Description

Low power

Blank Screen

Er1

Er2

Er3

Hi

Lo

Cause

Low power

Auto shutdown

Battery installation incorrectly

Low power

The screen is still blank

The environment temperature is out of range 10~40 ° C (33.8-

39.2

° F)

The environment temperature is not stable

Infrared module failure

The measurement is out of range > 42.2

° C (108 ° F)

The meaurment is out of range

<34 ° C (108 ° F)

Solution

Replace batteries

Restart the device

Check the correct installation of the batteries

Replace batteries

Contact service personnel

Move the device to appropriate environment and wait 30 minutes prior to taking a temperature.

Do not take measurement until the environment temperature is stable

Contact service personnel

Make sure the operation method is correct and the lens fi lter is new and clean. Remeasure.

Make sure the operation method is correct and the lens fi lter is new and clean. Remeasure.

7.2 Obtaining Technical Assistance

For technical information and assistance, or to order a service manual, call Huntleigh

Healthcare Ltd Service Department. The service manual includes information required by quali fi ed service personnel when servicing the Smartsigns ® Compact 300.

When calling the Huntleigh Healthcare Ltd Service Department, you may be asked to tell the representative the software version number of your equipment. Quali fi ed service personnel or Huntleigh Healthcare Ltd Service Department may help you check the software version installed in your equipment.

Make sure the environment in which the equipment is installed is not subject to strong sources of electromagnetic interference (e.g. radio transmitters, mobile phones).

This equipment generates and uses radio frequency energy. If not installed and used properly, in strict accordance with the manufacturer’s instructions, it may cause or be subject to interference. Type-tested in a fully con fi gured system, complies with EN60601-

1-2, the standard intended to provide reasonable protection against such interference.

Whether the equipment causes interference may be determined by turning the equipment off and on. If it does cause or is affected by interference, one or more of the following measures may correct the interference:

• Reorienting the equipment

• Relocating the equipment with respect to the source of interference

• Moving the equipment away from the device with which it is interfering

• Plugging the equipment into a different outlet so that the devices are on different branch circuits

WARNING: The use of accessories, transducers and cables other than those speci fi ed, with the exception of transducers and cables sold by the manufacturer of the Smartsigns® Compact 300 as replacement parts for internal components, may result in increased emissions or decreased immunity of the Smartsigns® Compact 300.

WARNING: The Smartsigns® Compact 300 should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary, the Smartsigns® Compact 300 should be observed to verify normal operation in the con fi guration in which it will be used

WARNING: Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the Smartsigns® Compact 300 including cables speci fi ed by the manufacturer. Otherwise, degradation of the performance of this equipment could result.

Guidance and Manufacturer’s declaration - electromagnetic emissions

The IRT10 infrared ear thermometer is intended for use in the electromagnetic environment speci fi ed below. The customer or the user of the IRT10 infrared ear thermometer should assure that it is used in such an environment.

Emissions Test Compliance

RF emissions

CISPR 11

Group 1

Electromagnetic Environment - guidance

The IRT10 infrared ear thermometer 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.

RF emissions

CISPR 11

Harmonic emissions

IEC 61000-3-2

Voltage fl uctuations / fl icker emissions

IEC 61000-3-3

Class A

Class A

Complies

The IRT10 infrared ear thermometer is suitable for use in all establishments, other than domestic and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

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The IRT10 infrared ear thermometer is intended for use in the electromagnetic environment speci fi ed below.

The customer or the user of the IRT10 infrared ear thermometer should assure that it is used in such an environment.

Immunity

Test

Guidance and Manufacturer’s declaration - electromagnetic immunity

IEC 60601 test level

Compliance level

Electromagnetic Environment - guidance

Portable and mobile RF communications equipment should be used no closer to any part of the

Smartsigns® Compact 300, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.

3 Vrms

150kHz to 80MHz outside ISM bands a

Conducted RF

IEC 61000-4-6 6 Vrms

150 kHz to 80 MHz in ISM and amateur radio bands

3V d = 1.2 √ P

Radiated RF

IEC 61000-4-3

3 V/m

80MHz to 2.5GHz

3V/m d = 1.2 √ P

80MHz to 800MHz d = 2.3 √ P

800MHz to 2.5GHz

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). b

Field strengths from fi xed RF transmitters, as determined by an electromagnetic site survey, c should be less than the compliance level in each frequency range d .

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

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

NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and re fl ection from structures, objects and people.

a The ISM (industrial, scienti fi c and medical) bands between 150 kHz and 80 MHz are 6,765 MHz, to 6,795

MHz; 13,553 MHz to 13,567 MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz.

b The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2,5 GHz are intended to decrease the likelihood that mobile/portable communications equipment could cause interference if it is inadvertently brought into patient areas. For this reason, an additional factor of 10/3 is used in calculating the recommended separation distance for transmitters in these frequency ranges.

c Field strengths from fi xed 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 fi xed RF transmitters, an electromagnetic site survey should be considered. If the measured fi eld strength in the location in which the IRT10 infrared ear thermometer is used exceeds the applicable RF compliance level above, the

IRT10 infrared ear thermometer should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the Smartsigns®

Compact 300.

d Over the frequency range 150kHz to 80kHz, fi eld strengths should be less than 3V/m.

Guidance and Manufacturer’s declaration - electromagnetic immunity

The IRT10 infrared ear thermometer intended for use in the electromagnetic environment speci fi ed below.

The customer or the user of the IRT10 infrared ear thermometer should assure that it is used in such an environment.

Immunity Test

Electrostatic discharge (ESD)

IEC 60601 test level

± 6 kV contact

± 8 kV air

Compliance level

± 6 kV contact

± 8 kV air

Electromagnetic Environment - guidance

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

IEC 61000-4-2

Electrical fast transient burst

± 2 kV for power supply lines

± 2 kV for power supply lines

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

IEC 61000-4-4

Surge

± 1 kV for input/ output lines

± 1 kV line(s) to line(s)

IEC 61000-4-5

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

IEC 61000-4-11

± 2 kV line(s) to earth

<5 % U r

(>95 % dip in U for 0,5 cycles r

40 % U r

(60 % dip in U r for 5 cycles

)

)

70 % U r

(30 % dip in U r for 25 cycles

)

± 1 kV for input/ output lines

± 1 kV line(s) to line(s)

± 2 kV line(s) to earth

<5 % U

40 % U

70 % U r r r

(>95 % dip in U for 0,5 cycles

(60 % dip in U for 5 cycles

(30 % dip in U for 25 cycles r r r

)

)

)

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

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

If the user of the IRT10 infrared ear thermometer requires continued operation during power mains interruptions, it is recommended that the IRT10 infrared ear thermometer is powered from an uninterruptible power supply or battery, by specifying the battery option at time of purchase.

<5 % U r

(>95 % dip in U r for 5 s

)

3 A/m

<5 % U r

(>95 % dip in U r for 5 s

)

3 A/m Power frequency

(50/60Hz) magnetic fi eld

Power frequency magnetic fi elds should be at levels characteristic of a typical location in a typical commercial or hospital environment.

IEC 61000-4-8

NOTE U r

is the a.c. mains voltage prior to the application of the test level.

19

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Recommended separation distances between portable and mobile RF communications equipment and the Smartsigns® Compact 300

The IRT10 infrared ear thermometer is intended for use in an electromagnetic environment in which radiated

RF disturbances are controlled. the customer or user of the IRT10 infrared ear thermometer can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the IRT10 infrared ear thermometer as recommended below, according to the maximum output power of the communications equipment.

Rated maximum output power of transmitter

Separation distance according to frequency of transmitter m

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

W d = 1.2 √ P d = 1.2 √ P d = 2.3 √ P

0.01

0.1

1

0.12

0.38

1.2

0.12

0.38

1.2

0.23

0.73

2.3

10 3.8

3.8

7.3

100 12 12 23

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (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 80MHz and 800MHz, 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 re fl ection from structures, objects and people.

9. Speci

fi

cations

9.1 Equipment Classi

fi

cation

Type of protection against electric shock.

Degree of protection against electric shock

Internally powered equipment

BF

Mode of operation.

Degree of protection against harmful ingress of particles and/or water.

Degree of safety of application in the presence of a fl ammable anaesthetic

Continuous

IPX1

Equipment not suitable for use in the presence of a

FLAMMABLE ANAESTHETIC MIXTURE WITH AIR,

OXYGEN OR NITROUS OXIDE

9.2 Standards

MDD 93/42/EEC

EN ISO14971: 2012

EN 60601-1-2: 2007/AC:2010

EN 980:2008

EN ISO10993-1:2009

EN ISO 10993-10:2010

EN 1060-3:1997+A2:2009

EN ISO 80601-2-30:2009+A1:2013

EN 62366:2008

9.3 General

Battery

Battery Life

Size

Weight

2 x Type LR03 AAA1.5VDC

3000 measurements

133 x 63.5 x 36.4 mm

80g

Automatic Shut down 60s±10s

Service Life 7 years

EN ISO13485:2012+AC2012

EN 60601-1: 2006/ AC:2013

EN60601-1-6:2010

EN 1041: 2008

EN ISO10993-5:2009

EN 1060-1:1995+A2:2009

EN 1060-4:2004

EN ISO 80601-2-61:2011

EN62304:2006

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9.4 Environmental

Operation

Temperature

Humidity

Altitude

15 °C to 36 °C (59 ° F to 96.8

≤ 85% non-condensing

700 hPa to 1060hPa

° F)

Transport and Storage

Temperature –25 °C to 55 °C (-13 ° F to 131 ° F)

Humidity ≤ 85% non-condensing

Altitude 700 hPa to 1060 hPa

Note: The system may not meet its performance speci fi cations if stored or used outside the manufacturer’s speci fi ed temperature and humidity range.

9.5 Measurement Parameters

Probe Type

Range

Accuracy

Resolution

Tympanic Infrared

34 °C to 42.2 °C (93.2 °F to 108°F)

35° C to 42° C (95 °F to 107.6°F) : ±0.2° C (±0.4° F)

Other Range : ±0.3° C (±0.5° F)

0.1°C (0.1

Measurement Interval ≥ 12s

° F)

Masurement duration 3s±1s

10. Warranty & Service

Huntleigh Healthcare Diagnostic Products Division standard terms and conditions apply to all sales. A copy is available on request. These contain full details of warranty terms and do not limit the statutory rights of the consumer.

10.1 Service Returns

If for any reason the Wireless Thermometer has to be returned, please:

• Clean the product following the instructions in this manual.

• Pack it in suitable packing.

• Attach a decontamination certi fi cate (or other statement declaring that the product has been cleaned) to the outside of the package.

• Mark the package ‘Service Department ‘

For further details, refer to NHS document HSG(93)26 (UK only).

Huntleigh Diagnostics reserve the right to return product that does not contain a decontamination certi fi cate.

A service manual is available for the Smartsigns ® series. It contains service information, parts lists and fault fi nding guidelines. The service manual can be obtained by contacting your local supplier or:-

Huntleigh Healthcare, Diagnostic Products Division,

Cardiff. CF24 5HN

Fax: 20492520

[email protected]

www.huntleigh-diagnostics.com

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Huntleigh Healthcare Ltd.

35 Portmanmoor Road, Cardiff, CF24 5HN, United Kingdom

T: +44 (0)29 20485885 F: +44 (0)29 20492520 [email protected]

www.huntleigh-diagnostics.com

Registered No: 942245 England & Wales. Registered Office:

ArjoHuntleigh House, Houghton Hall Business Park, Houghton Regis, Bedfordshire, LU5 5XF

©Huntleigh Healthcare Limited 2017

A Member of the Arjo Family

® and ™ are trademarks of Huntleigh Technology Limited

As our policy is one of continuous improvement, we reserve the right to modify designs without prior notice.

AW:1001008-3

781309EN-2