- American Diagnostic Corporation

e-sphyg 2
TM
9002
Automatic Sphygmomanometer
User’s
Manual
AMERICAN DIAGNOSTIC CORPORATION
1
A Special
Thank You...
Thank you for choosing an ADC® blood pressure instrument. We're proud of the
care and quality that goes into the manufacture of each and every item that bears our
name. Only the finest materials are used to assure you of a timeless instrument designed for optimum performance.
You'll quickly appreciate the results, for you now own one of the finest sphygmomanometers that money can buy.
With proper care and maintenance, your ADC® blood pressure instrument is sure
to provide you with many years of dependable service. Please read the following instructions and general information which will prove helpful in allowing you to enjoy your ADC®
product.
Advantages of Digital
Your new ADC® e-sphygTM 2 sphygmomanometer is intended to provide you
with all of the functionality of a traditional sphygmomanometer, with none of the problems associated with these devices. Using state-of-the-art technology, your esphygTM 2 sphygmomanometer will provide you with performance, versatility, and
reliability exceeding the most popular aneroid and mercurial instruments.
Its dual mode design will permit the instrument to fully measure a patient’s blood
pressure and pulse automatically. In manual mode, it allows you to use the time proven
auscultatory method to obtain blood pressure readings.
Thank you for your patronage. It is indeed our pleasure to serve you.
Sincerely,
American Diagnostic Corp.
©2017 AMERICAN DIAGNOSTIC CORP.
2
ADC® 9002 e-sphygTM 2
Table of Contents
Introduction and Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4
Warnings and Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5
Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
Product Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
Name and Function of Each Part . . . . . . . . . . . . . . . . . . . . . . . . . .7-8
Preparation for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-10
How to Assemble Wall Model . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11
How to Assemble Mobile Model . . . . . . . . . . . . . . . . . . . . . . . . . . .12
Cuff Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
Taking Blood Pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13-16
Memory Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
Error Displays and Troubleshooting . . . . . . . . . . . . . . . . . . . . .18-20
Care and Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .21
Wall Unit Parts and Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .22
Mobile Unit Parts and Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .23
Mobile Base Assembly Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .24
Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .25
Limited Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .26
Replacement Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .27
Technical Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .28-29
This manual is intended to assist the user in the safe and efficient operation of the Automatic
Sphygmomanometer 9002. The product must be used in accordance with the procedures
contained in this manual and must not be used for purposes other than those described herein.
It is essential to read and understand the entire manual.
3
Introduction and Intended Use
The 9002 digital ADC® e-sphygTM 2 sphygmomanometer is a digital sphygmomanometer intended for measurement of systolic and diastolic blood pressure
and pulse rate in adult patients, i.e., age 12 and above. This product is not designed for neonatal use. Inaccurate readings may result if it is used on a child's
arm.
Accuracy was evaluated during clinical studies in which results with the 9002
digital ADC® e-sphygTM 2 sphygmomanometer were compared with simultaneous auscultatory measurements obtained with a standard sphygmomanometer.
In these studies, the onset of the fourth (or fifth) Korotkoff sound was taken as
the diastolic pressure for the purpose of determining overall efficacy. A copy of
this study is available from ADC® on request. To ensure that accuracy is maintained, compare readings obtained with the 9002 digital ADC® e-sphygTM 2
sphygmomanometer with values measured by a trained observer using a manual
sphygmomanometer at least every 6 months.
Blood pressure measurements determined with this device are equivalent to those
obtained by a trained observer using the cuff stethoscope auscultatory method,
within the limits prescribed by the American National Standard, Manual, electronic,
or automated sphygmomanometers.
The 9002 digital ADC® e-sphygTM 2 sphygmomanometer has the ability to function according to its specifications in the presence of common arrhythmia such
as atrial or ventricular premature beats or atrial
fibrillation.
4
Warnings and Precautions
Warning - 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 - If luer lock connectors are used in the construction of tubing, there is a possibility that they
might be inadvertently connected to intravascular fluid systems, allowing air to be pumped into a blood
vessel. Immediately consult a physician if this occurs.
Warning - Do not allow a blood pressure cuff to remain on patient for more than 10 minutes when inflated above 10mmHg. This may cause patient distress, disturb blood circulation, and contribute to injury of peripheral nerves.
Warning - Safety and effectiveness with neonate cuff sizes 1 through 5 is not established.
Warning - For all blood pressure systems that can be wall mounted, ensure that the unit is securely
mounted prior to use to avoid damage to the instrument and potential patient injury.
Warning - Do not use the 9002 in an explosive environment such as where flammable
anesthetics exist or inside an oxygen chamber with strong electrostatic and electromagnetic fields e.g.,
mobile phones.
Warning - Use of this instrument on patients under dialysis therapy or on anticoagulant, antiplatelets,
or steroids could cause internal bleeding.
Warning - Do not use cuffs, AC adapters or batteries other than those included with this product or
replacement parts supplied by the manufacturer.
Warning - This system may fail to yield specified measurement accuracy if operated or stored in
temperature or humidity conditions outside the limits stated in the specifications section of this manual.
Warning - When using with an infant or child cuff, extra care must be taken to prevent over-inflation.
To prevent discomfort or injury to the patient, ensure preset pressure is not set above the desired level.
Warning -This product may contain a chemical known to the state of California to cause cancer, birth
defects, or other reproductive harm.
Caution - Federal law restricts this device to sale by or on the order of a physician or licensed healthcare practitioner.
Caution - To avoid any possibility of accidental strangulation, keep this unit away from children and
do not drape tubing around your neck.
Note - To obtain the greatest accuracy from your blood pressure instrument, it is recommended that
the instrument be used within a temperature range of 50°F (10°C) to 104°F (40°C), with a relative humidity range of 15-90% (non-condensing).
Note - All connectors and inflation system should remain connected to the device during storage to
avoid dust entering through the connector port.
5
Symbols
Symbol
Definition
Symbol
Read Operating Instructions
LATEX
Definition
Manufacturer’s Information
Not made with
Natural Latex
Temperature Limit
Humidity Limitation
Circumference Size
Type BF Equipment
Product Features
DUAL DISPLAY COLUMN LCD and SEGMENT LCD (Simulated Mercury Column)
The pressure can be read in the column LCD height and as digital value in the
segment LCD.
DUAL MEASUREMENT MODE "AUTO" and "MANUAL" Modes of Measurement
Determination of blood pressure can be made either automatically by the oscillometric
method or manually by the auscultatory method using a stethoscope.
MODE
AUTO
MANUEL
DEFLATION RATE
Maintained at 4.0 to 4.9mmHg/sec
Maintained at preset rates of:
2.5, 4.5 or 6.5mmHg/sec
MEMORY
Last measured result auto saved
N/A
Cuff Sizes (Auto Mode)
The Small Adult size cuff will accommodate arms of approximately 7.4 to 10.6 inches
(19.0 to 27.0 centimeters). A Small Adult cuff should be used on patients 12 or older
only (in auto mode).
The Adult size cuff will accommodate an upper arm circumference range of approximately 9.0 to 15.7 inches (23.0 to 40.0 centimeters).
The Large Adult size cuff will accommodate that of approximately 13.3 to 19.6 inches
(34.0 to 50.0 centimeters).
6
Name and function of each part
MAIN UNIT
SEGMENT LCD
INFLATION MARK
COLUMN LCD
DEFLATION
MARK
2mmHg
PULSE
MARK
1mmHg
BATTERY MARK
POWER MARK
PRESET PRESSURE KNOB
START/STOP BUTTON
AC INDICATOR
SET/MEMORY BUTTON
MODE SELECTOR
AIR CONNECTOR
AIR PLUG
AC ADAPTER JACK
MAIN POWER
SWITCH
O :OFF
I :ON
BATTERY
COMPARTMENT
COVER
BATTERY
CONNECTOR
ADAPTER PLUG
7
BATTERY PLUG
Name and function of each part
Cuff Sizes
SMALL ADULT
Arm circumferences of 7.4”-10.6”
(19.0-27.0cm)
ADULT
Arm circumferences of 9.0”-15.7”
(23.0-40.0cm)
LARGE ADULT
Arm circumferences of 13.3”-19.6”
(34.0-50.0cm)
LUER CONNECTOR
(Male Luer to Female Bladder Tube)
BLADDER TUBE
(Female Luer Connection)
COILED TUBING
AIR
CONNECTOR
ADCUFFTM
(to main unit)
AC ADAPTER
ADAPTER PLUG
RECHARGEABLE
NICKEL METAL HYBRID
(NiMH) BATTERY
INSTRUCTION
MANUAL
BATTERY PLUG
Other parts included depending upon model selected.
8
Preparation for Use
Connecting and Using the AC Adapter (All models)
Connect AC ADAPTER PLUG to AC ADAPTER JACK
Plug AC ADAPTER in the power socket.
AC INDICATOR is lit when AC ADAPTER is connected correctly.
ADAPTER
PLUG
Installing the RECHARGEABLE NiMH Battery (All models)
NOTE: The battery enclosed in the product package is not charged, and needs to be
charged for about 4 hours before use.
NOTE: Turn off the power and unplug AC ADAPTER
before inserting the battery. Make sure " O " side
of MAIN POWER SWITCH is pressed down.
(Fig. 1)
Remove BATTERY COMPARTMENT COVER by
loosening and removing the screw. (Fig. 1)
Connect BATTERY PLUG to BATTERY
CONNECTOR inside the battery compartment
and insert the battery. (Fig. 2)
(Fig. 2)
Put back BATTERY COMPARTMENT COVER and
close it by inserting and tightening the screw.
Connect AC ADAPTER PLUG and plug AC
ADAPTER in the power socket to charge the
battery. The battery is charged regardless of whether
the e-sphygTM 2 is powered on or off.
BATTERY PLUG
(Fig. 3)
Orange light of AC INDICATOR indicates that
the battery is being charged. (Fig. 3)
The battery is fully charged after approximately 4 hours.
Unplug AC ADAPTER after the light turns
green as it indicates the battery is charged.
9
The color of the AC INDICATOR
may switch to green and return to
orange if the 9002 is operated
while charging battery, however it
does not indicate a problem.
BATTERY MARK flashes in the segment LCD when the battery charge is low.
Only a few more measurements remain before the battery runs down.
The battery needs to be recharged when BATTERY MARK is displayed.
Measurement cannot be made.
NOTE: The rechargeable batteries may not be completely full after their initial charge or
when they have not been used for an extended period of time. This should be solved once
the unit has been used a few times and the batteries have been charged and discharged.
Battery life
Life of the rechargeable NiMH battery is approximately 2 years. However it may vary
depending on operating conditions. Replace the battery when BATTERY MARK is displayed often or when frequent charging of the battery becomes necessary.
Tips on prolonging the battery life
The device is powered by the AC ADAPTER when it is connected;
the installed battery is not used if the AC ADAPTER is connected.
• Remove the battery when operating the device with the AC ADAPTER for an extended period of time or when the battery does not need to be charged.
• Avoid charging the battery if it is not completely exhausted.
Do not forcefully remove the battery or pull out the plugs holding
cords and cables.
Use indicated AC Adapter and the battery only.
Contact your dealer if they are damaged.
POWER MARK
The device goes to energy saver mode when it is left turned on and not operated for
approximately 3 minutes. The mark will be displayed for an hour and then disappear.
Make sure to turn off the device by pressing "O " side of MAIN POWER SWITCH down
after each use especially when the device is powered by the battery.
The device activates from energy saver mode when either START/STOP button or
SET/MEMORY button is pressed. It is recommended to activate the device by pressing
SET/MEMORY button since the device could start inflation if START/STOP button is
pressed. Press START/STOP button again and stop inflation if the cuff is not wrapped
around arm.
10
How to Assemble Wall Model
1.
Securely attach wall bracket to flat surface using enclosed mollys and screws at desired height.
(It is advised to use a level to ensure proper mounting). (Figure 1)
2.
Attach manometer to wall bracket by lowering a top wall
bracket, sliding male tab into female seat of the bracket.
Secure the two together using the (6mm) allen bolt and
washer from below. Tighten securely with large (6mm)
allen wrench (Figure 2).
3.
4.
Figure 1
Securely attach cuff basket to flat surface to left of
manometer using enclosed mollys and screws at desired
height. (It is advised to use a level to ensure even mounting)
(Figures 3 - 4).
Attach 8 foot length coiled tubing to air inlet on face of
e-sphygTM 2 (Figure 5).
Insert “male” luer connector (891M) on free end of
coiled tubing to “female” luer connector (891F) on
bladder tubing (Figure 6). Fold cuff and store in basket.
Figure 2
300
290
280
270
260
250
2
80
130
82
40
e-sphyg
240
230
210
190
180
170
160
150
140
130
73
120
110
POWER
70
60
220
200
AC
PRESET PRESSURE
180
220 MANUAL
50
140
30
100
20
Figure 3
260
280
AUTO
10
SET/MEMORY
START/STOP
100
90
LOW BATTERY
POWER
80
70
60
AC
PRESET PRESSURE
180
220 MANUAL
50
140
30
100
40
20
260
280
AUTO
10
SET/MEMORY
Figure 4
START/STOP
Figure 5
Figure 6
11
How to Assemble Mobile Model
1.
With base on its side connect upright outer pole to base
using large (6mm) allen bolt. Tighten with large (6mm)
allen key provided. Tighten hardware as securely as
possible. (Note: To prevent loosening, hardware must be
tightened securely and periodically checked) (Figure 1).
2.
Slide spring and stainless steel inner pole inside outer
pole with open end up (Figure 2).
3.
Loosen (3mm) allen bolt on collar of cuff storage basket
with small (3mm) allen key provided. Place cuff storage
basket on top of stainless steel inner pole making sure
the pole goes completely inside collar and tighten allen
bolt with key (Figure 3).
4.
Attach manometer to basket using (6mm) allen bolt and
washer as shown. Tighten securely with large (6mm) allen
key (Figure 4).
5.
Connect tubing as noted in Wall configuration #4.
6.
Adjust height of manometer by loosening adjusting knob
and raising or lowering inner pole until gauge is at desired
height. Tighten adjusting knob by hand (Figure 5).
Figure 1
Figure 2
300
290
280
270
260
250
2
e-sphyg
240
230
220
210
200
130
82
190
180
170
160
150
140
130
73
120
110
100
90
LOW BATTERY
POWER
80
70
60
AC
PRESET PRESSURE
180
220 MANUAL
50
140
30
100
40
20
260
280
AUTO
10
SET/MEMORY
START/STOP
Figure 3
Figure 4
Figure 5
12
Cuff Connections
PLUG / PORT
CONNECTION
1.
AIR CONNECTOR
(Coiled Tubing)
Figure 1
Squeeze the middle of the plastic air connector on
the end of coiled tubing between thumb and
forefinger,and insert into the air connection port on
the face of the e-sphyg 2TM. Make sure connector
firmly “lock” snaps into the port (Figure 1).
Figure 2
2.
MALE
CONNECTOR
(Coiled Tubing)
Firmly insert male connector of coiled tubing into female connector at end of the AdcuffTM bladder tubing. Be sure the connectors are tight (Figure 2).
FEMALE CONNECTOR
(Bladder Tube)
Taking Blood Pressure (Auto Mode)
Turn on the device by pressing "I " side of MAIN POWER SWITCH.
Move MODE SELECTOR downward and set the device to "AUTO".
See page 15 for "MANUAL" measurement.
Set the initial inflation value with PRESET PRESSURE KNOB.
Select the pressure approximately 30 to 40 mmHg above
expected systolic pressure.
Pressure can be set between 100 mmHg and 280 mmHg.
Set the pressure at 180 mmHg if patient's systolic pressure is
difficult to predict.
The cuff is re-pressurized to a higher value if the preset
pressure is too low for blood pressure to be taken during cuff
deflation.
13
ARM CIRCUMFERENCE
Apply the cuff to patient's arm.
Choose the right size of cuff for
your patient. NOTE: Only these 3 cuffs
may be used in auto mode.
9.0 to 15.7 inches (23.0 to 40.0 cm)
13.3 to 19.6 inches (34.0 to 50.0 cm)
7.4 to 10.6 inches (19.0 to 27.0 cm)
CUFF SIZE
ADULT
LARGE ADULT
SMALL ADULT
The lower edge of the cuff should be about 1” (2 to 3 cm)
above the inner elbow and BLADDER TUBE should be over the
inner part of the arm, positioning the ARTERY MARK of the
cuff over the brachial artery.
Press the surface of the cuff to make sure that the hook and
loop adhesive fastens securely.
The cuff should be wrapped loosely enough so that two fingers can be placed between
the cuff and patient's arm. If the cuff is wrapped tighter or looser than this,
inaccurate blood pressure readings may result.
If your patient is wearing a shirt that might restrict circulation in his/her upper arm or
he/she rolls his/her sleeve up over the upper arm, the blood flow will be restricted,
preventing accurate measurement.
Press START/STOP button.
The cuff is inflated automatically after zero settings.
Pressurization stops when pressure reaches the preset pressure value and
pressure starts to descend.
Heart mark flashes in the segment LCD synchronizing detected pulse.
Deflation rate is displayed at the lower right corner of the segment LCD.
Press START/STOP button whenever the measurement
should be interrupted.
The device will stop during any course of measurement
procedure and rapidly exhaust air from the cuff.
Air is rapidly exhausted from the cuff as
measurement completes.
Blood pressure and pulse rate are displayed.
14
Turn off the device by pressing "O" side of MAIN POWER SWITCH.
The device will go to the energy saver mode after approximately
3 minutes if it is not turned off. See page 10.
Make sure your patient is relaxed, has taken at least 5 minutes of rest before measurement and refrains from talking or moving during measurement.
Confirm that the cuff is kept at the height of patient's heart during measurement.
Do not execute repeated measurements for congestion of blood could result in false
measurement. Allow the patient's arm to rest for at least 5 minutes.
Taking Blood Pressure (Manual Mode)
When you want to take your patient's blood pressure using the auscultatory method
with a stethoscope, set the device to "MANUAL" mode.
Turn on the device by pressing " I " side of MAIN POWER SWITCH.
Move MODE SELECTOR upward and set the device to "MANUAL".
See page 13 for “AUTO” measurement.
Set the initial inflation value with PRESET PRESSURE KNOB.
Details on preset pressure … page 13.
Press SET/MEMORY button to confirm and/or select the
appropriate deflation rate.
The deflation rate is displayed at the lower right corner of the
segment display.
The deflation rate can be selected from 2.5, 4.5 and 6.5 mmHg/s.
The set deflation rate returns to the default value (2.5) when the
device is turned off.
15
Apply the cuff and stethoscope to the patient's arm in the same
manner as the usual auscultatory method.
Press START/STOP button.
The cuff is inflated automatically after zero settings.
Pressurization stops when pressure reaches the preset pressure value and
pressure starts to descend.
Deflation rate is displayed at the lower right corner of the segment LCD.
NOTE: Press START/STOP button whenever the measurement
should be interrupted. The device will rapidly exhaust air from the cuff.
If cuff inflation was not sufficient, press and hold down
START/STOP button once deflation has started and the cuff
is pressurized again. Pressurization will continue while the
button is pressed. Pressure does not exceed 290 mmHg.
Press START/STOP button when blood pressure is taken and air
is rapidly exhausted from the cuff.
Air is also rapidly exhausted from the cuff when pressure
descends to 30 mmHg.
Turn off the device by pressing "O" side of MAIN POWER SWITCH.
The device will be in the energy saver mode after approximately
3 minutes if it is not turned off. See page 10.
Make sure your patient is relaxed, has taken at least 5 minutes of rest before
measurement, and refrains from talking or moving during measurement.
Confirm that the cuff is kept at the height of patient's heart during measurement.
Do not execute repeated measurements for congestion of blood could result
in false measurement. Allow the patient's arm to rest for at least 5 minutes.
16
Memory Function
Measured result obtained in "AUTO" mode is automatically saved
in the memory and can be recalled until next measurement is taken.
The result is not saved when the measurement is performed
in "MANUAL" mode.
To recall the result, turn on the device by pressing "I" side of
MAIN POWER SWITCH and set the device to "AUTO" with
MODE SELECTOR.
Press SET/MEMORY button and the last
result from "AUTO" measurement is displayed.
Turn off the device by pressing "O" side of MAIN POWER SWITCH.
The device will be in the energy saver mode after approximately
3 minutes if it is not turned off. See page 10.
17
Error Displays and Troubleshooting
ERROR SYMBOL/SYMPTOM
CAUSE
REMEDY
OVER-PRESSURIZATION:
The cuff was inflated to the
maximum pressure because
of movement of body, etc.
Make sure that the patient stays
still during measurement.
MEASUREMENT ERROR:
Measurement could not be
made because of moving or
talking during measurement.
Make sure the patient remains
still and quiet during measurement.
INFLATION ERROR: AIR PLUG
is not correctly inserted.
Reinsert AIR PLUG and make
sure that it is securely inserted.
Noise was detected.
Make sure that the patient stays
still and quiet during
measurement.
DEFLATION ERROR:
Movement or talking was detected during measurement.
Make sure the patient remains
still and quiet during
measurement.
Extreme changes in pressure
occurred during measurement.
Do not let patient move during
measurement.
CHECKING MODE:
See page 21.
Turn off the device once and
then turn it on again to take
measurement.
NO POWER:
AC ADAPTER is not
correctly connected.
Battery is exhausted.
Nothing is being dis9002 was left turned on but
played when MAINhas not been operated for over
POWER SWITCH is
an hour.
pressed down in the ON
position.
18
Reinsert AC ADAPTER and
make sure that it is securely
inserted.
Charge the battery or use AC
ADAPTER.
Turn off the device or press
START/STOP button or
SET/MEMORY button to activate the device from energy
saver mode.
Error Displays and Troubleshooting
ERROR SYMBOL/SYMPTOM
CAUSE
REMEDY
LOW BATTERY:
Battery is weak.
Change the battery. Only a
few measurements can be
made before the battery runs
down.
BATTERY ERROR:
Charge the battery.
The indication appearing
during LCD segment test,
which is performed when
the unit is turned on, does
not indicate low battery or
battery error.
ENERGY SAVER MODE:
The device was left turned
on and has not been operated for over approximately
3 minutes.
Measurement is interrupted once and the cuff
is inflated again.
When the preset pressure
value was not high enough
to make measurement or
when noise was detected,
the cuff is pressurized
again to a higher level.
Charge the battery. Measurement cannot be conducted.
Turn off the device or press
START/STOP button or
SET/MEMORY button to activate the device from energy
saving mode. Make sure to
turn off the device by pressing “o” side of MAIN POWER
SWITCH after use.
This does not indicate a
problem.
Patient moved during
measurement.
Make sure that the patient
stays still and quiet during
measurement.
Blood pressure is different each time. The reading is extremely low (or
high)
Patient is not being measured with correct posture.
Blood pressure readings
constantly vary with time
of measurement and physical and mental condition.
Make sure that the patient is
being measured with correct
posture.
Pulse rate is too low (or
too high).
Patient moved during
measurement. There was
not enough rest taken
before measurement.
Make sure that the patient
stays still during measurement. Allow your patient to
rest for at least 5 minutes.
19
Error Displays and Troubleshooting
ERROR SYMBOL/SYMPTOM
CAUSE
REMEDY
Measurement result cannot be recalled or is not
stored.
Blood pressure was taken
in“MANUAL” mode.
Measurement result is saved
only when it is taken in “AUTO”
mode.
Cuff inflation does not
start.
Battery is exhasted
Measurement cannot be made
when BATTERY MARK is displayed. Recharge the battery.
AC INDICATOR is lit even
when 9002 is turned off.
Battery is inserted.
The column LCD is dim
or brightness is not
steady.
9002 is operated with the
battery.
AC INDICATOR also indicates
whether the battery is being
charged or it is not being
charged.
Difference in voltages between
AC ADAPTER and the battery
lead to differences in LCD
brightness. This does not indicate a functional problem.
If you cannot get correct measurement with the methods above, do not tamper
with the internal mechanism. Contact your dealer. If the unit malfunctions, return it to the dealer or an authorized service representative for servicing according to the warranty. The manufacturer provides service data to qualified dealers.
20
Care and Maintenance
Because the device includes precision parts, care should be taken to avoid extreme temperature variations, humidity, shock, dust, and direct sunlight. Do not
drop or strike the device. Make sure not to expose the unit to moisture. This
unit is not water resistant.
Use only a soft, dry cloth to clean the device. Do not use gasoline, paint thinner,
chemicals such as strong bases, strong acids, oxidizing agents, and reducing
agents, or other strong solvents on the unit. Since the cuffs may absorb perspiration and other fluids, inspect them for stains and discoloration after each use.
Sponge with a damp cloth. If necessary the cuff can be washed in cool water
with mild soap or detergent-disinfectant. Remember to remove the bladder prior
to washing. After washing, the cuff should be rinsed and allowed to air dry.
NEVER iron.
When storing the device, do not place heavy objects on it and do not coil BLADDER
TUBE too tightly. When the unit has been stored at a temperature below the
freezing point, keep it for at least 1 hour in a warm place before using. Remove
the battery if the device is to be stored for an extended period of time. Keep the
batteries out of the reach of children.
Caution: Do not inflate the cuff when it is not wrapped around an arm.
Caution: Do not disassemble or modify the device.
We suggest that the device be checked every 2 years. This operation may only
be performed by the manufacturer or by firms authorized by the manufacturer.
Checking pressure accuracy
Connect a cuff wrapped around a firm cylinder to the 9002
e-sphygTM 2 and a standard manometer. Turn on the 9002
e-sphygTM 2 while pressing and holding the START/STOP button down. Release the button after the initial display (all segment
display) disappears. Two "0"s are displayed and the 9002 esphygTM 2 is in CHECKING MODE. Inflate the cuff with an inflation bulb and compare the readings. Pressure accuracy is to be
±3mmHg. Contact dealer if accuracy of your 9002 e-sphygTM 2
is invalid.
(A test kit may be purchased from an authorized dealer)
21
9002
e-sphygTM 2
BLADDER
TUBE
9002
PORT
9002W - Wall Unit Parts & Tools
1.
ADC Item
Item no.
e-sphygTM 2
9002
1
300
290
280
270
260
250
2
e-sphyg
240
230
2.
6mm Allen Wrench
220
752M-116
210
200
130
82
190
180
170
3.
Wall Bracket
160
952-103
150
140
130
110
4.
Wall Basket with
(3) screws / (3) mollys
2
73
120
100
90
80
70
AC
PRESET PRESSURE
180
220 MANUAL
60
952-025
752M-116
LOW BATTERY
POWER
50
140
30
100
40
260
20
280
AUTO
10
5.
Coiled tubing
885N
6.
Mounting Bolt/Washer (1)
972-101
7.
Connector
9002-2
8.
Connector, Male
891M
9.
Connector, Female
SET/MEMORY
START/STOP
9002
891F
3
10. AdcuffTM & Bladder, Adult
845-11AN-1F
11. (2) Screws (for wall bracket)
952-104
12. (2) Mollys (for wall bracket)
952-105
952-103
4
952-025
6
11
8
972-101
10
891M
5
952-104
SELECT CUFF
R
LARGE
X
E / MA
RANG
ADCUFF
9
7
ARTERY
ADULT SIZE
885N
9002-2
891F
845-11AN-1F
22
12
952-105
9002M - Mobile Unit Parts & Tools
ADC Item
Item no.
1.
e-sphygTM 2
9002
2.
6mm Allen Wrench
752M-116
3.
3mm Allen Wrench
752M-117
1
300
290
2
280
270
260
250
2
e-sphyg
240
230
220
210
4.
Mounting Bolt/Washer (2)
200
972-101
170
160
150
5.
Mobile Stand
752M-02
6.
Coiled tubing
885N
752M-116
130
82
190
180
140
130
73
120
110
100
90
LOW BATTERY
POWER
80
70
60
AC
PRESET PRESSURE
180
220 MANUAL
50
140
30
100
40
260
20
7.
Connector
9002-2
8.
Connector, Male
891M
9.
Connector, Female
891F
280
SET/MEMORY
10. AdcuffTM & Bladder, Adult
AUTO
10
START/STOP
752M-117
9002
3
845-11AN-1F
4
972-101
7
9002-2
5
10
6
SELECT CUFF
R
LARGE
E
RANG
X
/ MA
ADCUFF
752M-02
8
9
ARTERY
ADULT SIZE
891M
885N
23
891F
845-11AN-1F
Mobile Base Assembly Parts
9
8
9B
5
2
7
4
3
1
6
6A
3A
ADC Item
Item no.
1 Center Pole Screw (1)
Washer (1)
972-101
2 Base
972-080
ADC Item
6
Spring
Item no.
972-109
6A Gasket, Rubber
972-107A
7
Inner Pole
972-110
3 Casters (5)
972-106
8
Basket Tightening Key
972-111
3A Single Caster
972-106-1
9
Basket
972-112
4 Outer Pole
972-107
5 Knob
972-108
9B Manometer Mounting
Hardware
24
752-114
Specifications
Operating Principle:
Indicator:
Pressure Indicating Range:
Measuring Range:
Accuracy:
Inflation :
Deflation:
Exhaust:
Power Supply:
Power Consumption :
Memory:
Operating Environment:
Storage Environment:
Oscillometric method*
300 digits column LCD and 10 digits segment LCD
0 to 300 mmHg (cuff pressure)
50 to 250 mmHg (systolic)
40 to 180 mmHg (diastolic)
40 to 160 bpm (pulse rate)
±3 mmHg (cuff pressure)
±5% of reading (pulse rate)
Automatic inflation
Electric control valve
Automatic exhaust valve
Power Supply: 7.0 VDC AC Adapter (Model UM318-0725 or
4.8 VDC Rechargeable Ni-MH Battery
Adapter I/P: AC100-240V
14W (max.)
single measurement result*
+50°F to+104°F, 15 to 85% relative humidity
-4°F to+140°F, 15 to 85% relative humidity
Coverage Arm Circumference
Adult Size Cuff:
Large Adult Size Cuff:
Small Adult Size Cuff:
9.0 to 15.7 inches (23.0 to 40.0 cm)
13.3 to 19.6 inches (34.0 to 50.0 cm)
7.4 to 10.6 inches (19.0 to 27.0 cm)
Main Unit
Weight:
Size:
Approx. 2.2 lb. [1000 g], without AC adapter or battery
5.4 x 10.6 x 3.8 in [136 x 266 x 96 mm] (W x D x H)
Specifications are subject to change without notice due to improvements in performance.
* marks only apply to "AUTO" measurement.
25
Limited Warranty
American Diagnostic Corporation (ADC®) warrants its products against defects in materials and workmanship under normal use and service as follows:
1. Warranty service extends to the original retail purchaser only and commences
with the date of delivery.
2. The entire sphygmomanometer is warranted for two years.
3. Cuff, bladder and coiled tubing are warranted for three years.
4. The manometer is warranted to remain accurate to ±3mmHg over its full
range when compared to a reference standard for life.
What is Covered: Repair, or replacement of parts, and labor.
What is not covered: Transportation charges to and from ADC®. Damages caused by abuse,
misuse, accident, or negligence. Incidental, special, or consequential damages. Some states
do not allow the exclusion or limitation of incidental,
special, or consequential damages, so this limitation may not apply to you.
To Obtain Warranty Service: Send item(s) postage paid to ADC®, Attn: Service Dept., 55 Commerce Dr., Hauppauge, NY 11788. Please include your name and address, daytime phone
no., proof of purchase, a brief note explaining the problem, and $2.00 to cover the cost of
return shipping and handling.
Implied Warranty: Any implied warranty shall be limited in duration to the terms of this warranty and in no case beyond the original selling price (except where
prohibited by law). This warranty gives you specific legal rights and you may have other
rights which vary from state to state.
To Register Your Product, visit us at
www.adctoday.com/register
26
Replacement Parts
Part No. Latex-free
Model Use
Coiled Tubing 4’
Component
886N
Desk
Coiled Tubing 8’
885N
Mobile, Wall
Cuff & Bladder - Sm. Adult
845-10SARB-1F
All Models
Cuff & Bladder - Adult
845-11AN-1F
All Models
Cuff & Bladder - Lg. Adult
845-12XBD-1F
All Models
Female Luer Connector
891F
All Models
Male Luer Connector
891M
All Models
Plastic Connector
9002-2
All Models
AC Adapter
9002-3
All Models
Rechargeable Battery Pack
9002-5
All Models
FOR QUESTIONS, COMMENTS,
OR SUGGESTIONS
CALL TOLL FREE: 1-800-ADC-2670
OR VISIT
WWW.ADCTODAY.COM/FEEDBACK
Many ADC instruction manuals are available on our website in other languages at
www.adctoday.com/care
©2017 ADC®. All rights reserved. No one is permitted to reproduce or duplicate in any form, this manual
or any part thereof without the expressed written permission of ADC®. ADC® 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 the product in accordance with the instructions, cautions, warnings, or statement of intended
use published in this manual. The 9002 e-sphyg 2TM and AdcuffTM are trademarks of ADC®.
27
Technical Description
The 9002 complies with the EMC, electromagnetic compatibility, standard, IEC60601-1-2. Refer to the tables below for specific information regarding compliance to the standard.
The 9002, as a medical electrical equipment, needs special precautions regarding EMC and needs to be installed and put into
service according to
the EMC information provided below.
Portable and mobile RF communications equipments can affect the device.
The use of accessories other than those specified in this manual may result in increased emissions or decreased immunity of
the device.
The 9002 should not be used adjacent to or stacked with other equipment.
Table 1 - Guidance and manufacturer’s declaration - electromagnetic emissions The 9002 is intended for use in the electromagnetic environment specified below.
The customer or the user of the 9002 should assure that it is used in such an environment.
Compliance Electromagnetic environment - guidance
The 9002 uses RF energy only for its internal function. Therefore, its RF emissions are
Group 1
very low and are not likely to cause any interference in nearby electronic equipment.
Emissions test
RF emissions CISPR 11
RF emissions CISPR 11
Harmonic emissions IEC 61000-3-2
Voltage fluctuations/flicker emissions
IEC 61000-3-3
Class B
Class A
N/A
The 9002 is suitable for use in all establishments, including domestic establishments and directly connected to the public low-voltage power supply network that supplies buildings used for
domestic purposes.
Table 2 - Guidance and manufacturer’s declaration - electromagnetic immunity The 9002 is intended for use in the electromagnetic environment specified below.
The customer or the user of the 9002 should assure that it is used in such an environment.
Immunity test
IEC 60601 test level
±6 kV contact
±8 kV air
Compliance level
±6 kV contact
±8 kV air
Electrical fast
transient/burst IEC
61000-4-4
±2 kV for power supply lines
±1 kV for input/ output lines
±2 kV for power supply lines
±1 kV for input/ output lines
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.
Surge IEC 61000-4-5
±1 kV differential mode
±2 kV common mode
±1 kV differential mode
±2 kV common mode
Mains power quality should be that of a
typical commercial or hospital environment.
Voltage dips, short
interruptions and voltage
variations on power supply
lines IEC 61000-4-11
<5% UT (>95% dip in UT) for 0,5 cycle
40% UT (60% dip in UT) for 5 cycles
70% UT (30% dip in UT) for 25 cycles
<5% UT (>95% dip in UT) for 5 sec
<5% UT (>95% dip in UT) for 0,5 cycle
40% UT (60% dip in UT) for 5 cycles
v70% UT (30% dip in UT) for 25 cycles
<5% UT (>95% dip in UT) for 5 sec
Mains power quality should be that of a typical
commercial or hospital environment. If the user
of the 9002 requires continued operation during
power mains interruptions, it is recommended
that the 9002 is to be powered from an
uninterruptable power supply or a battery.
Power frequency
(50/60 Hz) magnetic
field IEC 61000-4-8
3 A/m
3 A/m
Power frequency magnetic fields should be at
levels characteristic of a typical location in a
typical commercial or hospital environment.
Electrostatic discharge
(ESD) IEC
61000-4-2
NOTE UT is the a.c. mains voltage prior to application of the test level.
28
Electromagnetic environment - guidance
Table 4 - Guidance and manufacturer’s declaration - electromagnetic immunity The 9002 is intended for use in the electromagnetic environment specified below.
The customer or the user of the 9002 should assure that it is used in such an environment.
Immunity test
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 9002, including cables,
than the recommended separation distance calculated from
the equation applicable to the frequency of the transmitter.
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3 Vrms
150 kHz to 80 MHz
3 Vrms
80 MHz to 2,5 GHz
3 Vrms
Recommended separation distance
d=[3,5/V1] P
3 Vrms
d=[3,5/E1] P 80 MHz to 800 MHz
d=[7/E1] 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 meters (m).
Field strengths from fixed RF transmitters, as determined by a 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.
Field strength from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radios
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 9002 is used exceeds the applicable RF compliance level
above, the 9002 should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or
relocating the 9002.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
a
Table 6 - Recommended separation distances between portable and mobile RF communications equipment and the 9002 The 9002 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of
the 9002 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications
equipment (transmitters) and the 9002 as recommended below, according to the maximum output power of the communications equipment.
Rated maximum output
Separation distance according to frequency of transmitter, m
power of transmitter, W
150 kHz to 80 MHz, d=[3.5/V1] P
80 MHz to 800 MHz, d=[3.5/E1] P
800 MHz to 2.5 GHz, d=[7/E1] P
0.01
0.12
0.12
0.23
0.1
0.38
O.38
0.73
1
1.2
1.2
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 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.
NOTE1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures,
objects and people.
29
ADC
55 Commerce Drive
Hauppauge, NY 11788
U.S.A.
Inspected, Assembled and Packaged in the U.S.A.
Made in Japan
tel: 631-273-9600, 1-800-232-2670
fax: 631-273-9659
www.adctoday.com
email: info@adctoday.com
IB p/n 93-9002-00 rev 11
Printed in Japan
A114487-1_7
30
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