ADC e-sphyg 2 User manual

e-sphyg TM 2
9002
Automatic Sphygmomanometer
AMERICAN DIAGNOSTIC CORPORAT I O N
User’s
Manual
ADC
55 Commerce Drive
Hauppauge, NY 11788
ADC (UK) Ltd.
Unit 6, PO14 1TH
United Kingdom
Inspected in the U.S.A.
Made in Japan
tel: [phone]
fax: [phone]
w w w. a d c t o d a y. c o m
email: [e-mail]
IB p/n 93-9002-00 rev 3 Printed in Japan
0197

2 27
A Special
Thank Yo u . . .
Thank you for choosing an ADC®blood pressur e 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
instr ument designed for optimum perfor m ance.
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 pressur e instrument is sure
to provide you with many years of dependable service. Please read the following
instr uctions and general information which will prove helpful in allowing you to
enjoy your ADC®pro d u ct.
Advantages of Digital
Your new ADC®e-sphygTM 2sphygmomanometer is intended to provide you
with all of the functionality of a traditional sp h ygmom a n ometer, with none of the
problems associated with these devices. Using state-of-the-art technology,
your e-sphygTM 2sphy g moman o mete r will provide you with p e rfo rmance,
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 pre ssur e and pulse automatically. In manual mode, it allows you to use
the time proven auscultatory method to obtain blood pres sure readi ngs.
Thank you for your patronage. It is indeed our pleasure to serve you.
Sincerely,
American Diagnostic Corp.
©2006 AMERICAN DIAGNOSTIC CORP.
FOR QUESTIONS, COMMENTS,
OR SUGGESTIONS
CALL TOLL FREE: 1-800-ADC-2670
©2006 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 2
TM
and Adcuff
TM
are trade-
marks of ADC
®
.
Component Part No. Latex Part No. Latex-free Model Use
Coiled Tubing 4’ 886 886LF Desk
Coiled Tubing 8’ 885 885LF Mobile and Wall
Cuff & Bladder - Child 850FC 850FCLF All Models
Cuff & Bladder - Adult 850F 850FLF All Models
Cuff & Bladder - Lg. Adult 850FX 850FXLF All Models
Female Luer Conncetor N/A 891F All Models
Male Luer Conncetor N/A 891M All Models
Plastic Connector N/A 9002-2 All Models
AC Adapter N/A 9002-3 All Models
Rechargeable Battery Pack N/A 9002-5 All Models
Replacement Parts

26 3
ADC®9002 e-sphygTM 2
Table of Contents
In troduction and Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4
Wa rnings and Precaut io ns . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5
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 . . . . . . . . . . . . . . . . . . . . . . . . . . .1 2
Cu ff Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 3
Taking Blood Pre ss ure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 3- 16
M e m o ryFunction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
Error Displays and Troubl es ho oti ng . . . . . . . . . . . . . . . . . . . . .18- 20
Ca re and Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 1
Wall Unit Parts and To ol s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 2
Mobile Unit Parts and Too ls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .23
Mobile Base Assembly Part s . . . . . . . . . . . . . . . . . . . . . . . . . . . . .24
Sp ecifi ca ti ons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .25
Limited Wa rrant y . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .26
Replacement Part s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .27
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.
American Diagnostic Corporation (ADC
®
) warrants its products against defects in
materials and workmanship under norma l use and service as follows:
1. Wa r ranty service extends to the original retail purchaser only and commences
with the date of delivery.
2. The entire sphygmomanometer is warranted for one year.
3. Cuff, bladder and coiled tubing are warranted for two 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: R e p air, or replacement of parts, and labor.
What is not covered: Tr ansportation 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 Serv i ce: Send item(s) postage paid to ADC
®
, Attn: Service Dept.,
55 Commerce Dr., Hauppauge, NY 11788. Please include your name and addre s s,
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 Warra n t y : 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.adct oday.co m
and follow the links
Limited Warranty

4 25
Introduction and Intended Use
The 9002 digital ADC®e-sphygTM 2sphygmomanometer 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 2sphygmomanometer 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 2sphygmomanometer
with values measured by a trained observer using a manual
sphygmomanometer at least every 6 months.
Blood pre s s u r e 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 2sphygmomanometer 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.
Sp ec i fi ca t io ns
Operating Principle: Oscillometric method*
Indicator: 300 digits column LCD and 10 digits segment LCD
Pressure Indicating Range: 0 to 300 mmHg (cuff pres s u re)
Measuring Range: 50 to 250 mmHg (systolic)
40 to 180 mmHg (diastolic)
40 to 160 bpm (pulse rate)
Accuracy: ±3 mmHg (cuff pressure )
±5% of reading (pulse rate)
Inflation : Automatic inflation
Deflation: Electric control valve
Exhaust: Automatic exhaust valve
Power Supply: 7.0 VDC AC adapter (MODEL 9605+02225-1UOC) or
4.8 VDC rec h a rgeable NiMH battery
Power Consumption : 14W (max.)
Me m o ry: single measurement re s u l t *
Operating Environment: +50°F to+104°F, 15 to 90% relative humidity
Storage Environ m e n t : -4°F to+122°F, 15 to 95% relative humidity
Coverage Arm Circ u m f e rence
Adult Size Cuff: 10.28 to 16.1 inches (26.1 to 40.9 cm)
Large Adult Size Cuff: 13.5 to 20.04 inches (34.3 to 50.9 cm)
Child Size Cuff: 7.48 to 10.71 inches (19.0 to 27.2 cm)
Main Unit
Wei g h t : Approx. 2.2 lb. [1000 g], without AC adapter or battery
Size: 5.4 x 10.6 x 3.8 in [136 x 266 x 96 mm] (W x D x H)
This device complies with EMC (IEC60601-1-2), EN1060-1 and EN1060-3.
Specifications are subject to change without notice due to improvements in perfo rm anc e.
* marks only apply to "AUTO" measurem en t.

24 5
Warnings and Precautions
Wa r n i n g
•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.
Wa r n i n g
•Use of this instrument on patients under dialysis therapy or on
anticoagulant, antiplatelets, or steroids could cause internal bleeding.
Wa r n i n g
•Do not use cuffs, AC adapters or batteries other than those included
with this product or replacement parts supplied by the manufacturer.
Wa r n i n g
•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.
C a u t i o n
• To avoid any possibility of accidental strangulation, keep this unit
away from children and do not drape tubing around your neck.
C a u t i o n
•The standard material used for the bladder, inflation bulb, and coiled
tubing is natural rubber latex and it may cause allergic reactions.
Latex-free options are available.
N o t e
• 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).
N o t e
• All connectors and inflation system should remain connected to the
device during storage to avoid dust entering through the connector port.
1
2
3
4
5
6
7
8
7A
9
10
10B
ADC Item Item no.
1 Center Pole Screw (1)/Washer (1) 97 2 -10 1
2 Legs (5) 972 - 103
3 Leg Screws (5) 972 - 104
4 Casters (5) 972 - 106
5 Outer Pole 972 - 107
6Kno b 9 72-1 0 8
7Spr i ng 972 - 109
Mobile Base Assembly Parts
ADC Item Item no.
7A Gasket, Rubber 972 - 107A
8 Inner Pole 972 - 110
9 Basket Tightening Key 972 - 111
10 Ba s ket 972 - 112
10B Manometer Mounting Hardwa r e972- 1 01
N/A Complete 5 Leg Base 972 - 080
N/A Single Caster 97 2 -10 6 -1

6 23
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.
Cuff Sizes (Auto Mode)
The Child size cuff will accommodate arms of approximately 7.48 to 10.71
inches (19 to 27.2 centimeters). A child 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 10.28 to 16.1 inches (26.1 to 40.9 centimeters).
The Large Adult size cuff will accommodate that of approximately 13.5 to
20.04 inches (34.3 to 50.9 centimeters).
Cuff Sizes (Manual Mode)
In manual mode, any of ADC’s®5 cuff sizes (infant, child, adult, large adult or
thigh) may be used, on any patient.
Operation with AC Adapter or Rechargeable Battery
The digital ADC®e - s p h y g TM 2sphygmomanometer is powered by either an AC
Adapter or rechargeable nickel metal hybrid (NiMH) battery (both included).
MODE DEFLATION RATE MEMORY
AUTO Maintained at 4.0 to 4.9mmHg/sec Last measured result auto saved
Maintained at preset rates of:
2.5, 4.5 or 6.5mmHg/sec
MANUAL
7 5 2 M - 11 6
7 5 2 M - 11 7
9 0 0 2
7 5 2 M - 0 2
9002M - Mobile Unit Parts & Tools
8 8 5 8 5 0 F
9 0 0 2 - 2
8 9 1 M 8 9 1 F
1
2
3
4
5
6
7 9 7 2 - 1 0 1
8 9
10
N/A
ADC Item Item no.
1. e-sphygTM 29002
2. 6mm Allen Wre n c h 752M- 1 1 6
3. 3mm Allen Wre n c h 752M- 1 1 7
4. Mounting Bolt/Washer (2) 972-1 0 1
5. Mobile Stand 752M- 0 2
6. Coiled tubing 8 85
7. Conne c tor 900 2 - 2
8. Conne c tor, Male 891M
9. Conne c tor, Female 891F
10. A d c u ffT M & Bladder 850F

22 7
Name and function of each part
MAIN UNIT
COLUMN LCD
2mmHg
1mmHg
PRESET PRESSURE KNOB
START/STOP BUTTON
SET/MEMORY BUTTON
AIR CONNECTOR
AC INDICATOR
MODE SELECTOR
AIR PLUG
POWER MARK
BATTERY MARK
PULSE
MARK
DEFLATION
MARK
INFLATION MARK
SEGMENT LCD
AC ADAPTER JACK
MAIN POWER
SWITCH
O:OFF
I:ON
ADAPTER PLUG
BATTERY
CONNECTOR
BATTERY
COMPARTMENT
COVER
BATTERY PLUG
9002W - Wall Unit Parts & Tools
ADC Item Item no.
1. e-sphygTM 29002
2. 6mm Allen Wre n c h 75 2 M -116
3. Wall Bracket 95 2 - 103
4. Wall Basket with
(3) screws / (3) mollys 952-0 2 5
5. Coiled tubing 8 8 5
6. Mounting Bolt/Washer (1) 972-1 0 1
7. Conne c tor 900 2 - 2
8. Conne c tor, Male 891M
9. Conne c tor, Female 891 F
10. Adc u ffTM & Bladder 850F
11. (2) Screws (for wall bracket) 952-1 0 4
12. (2) Mollys (for wall bracket) 952-1 0 5
7 5 2 M - 11 6
9 0 0 2
9 5 2 - 1 0 3
9 5 2 - 0 2 5
8 8 5 8 5 0 F
9 0 0 2 - 2
8 9 1 M
8 9 1 F
1
2
3
4
5
6
9 7 2 - 1 0 1
7
8
9
10
1 2
9 5 2 - 1 0 5
11
9 5 2 - 1 0 4

8 21
Name and function of each part
CHILD (small adult)
Arm circumferences of 7.48”-10.71”
(19.0-27.2cm)
ADULT
Arm circumferences of 10.28”-16.1”
(26.1-40.9cm)
LARGE ADULT
Arm circumferences of 13.5”-20.04”
(34.3-50.9cm)
AC ADAPTER RECHARGEABLE
NICKEL METAL HYBRID
(NiMH) BATTERY
INSTRUCTION
MANUAL
ADAPTER PLUG BATTERY PLUG
Cuff Sizes
AIR
CONNECTOR
(to main unit)
ADCUFFTM
BLADDER TUBE
(Female Luer Connection)
COILED TUBING
LUER CONNECTOR
(Male Luer to Female
Bladder Tube)
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 thin-
ner, chemicals such as strong bases, strong acids, oxidizing agents, and reduc-
ing agents, or other strong solvents on the unit. Since the cuffs may absorb per-
spiration 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 blad-
der 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 - s p h y g TM 2and a standard manometer. Turn on the 9002
e - s p h y g TM 2while 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 e - s p h y g TM 2is
in CHECKING MODE. Inflate the cuff with an inflation bulb and
compare the readings. Pressu r e accuracy is to be ±3mmHg.
Contact dealer if accuracy of your 9002 e - s p h y g TM 2is invalid.
As a convenience to our customers, a test kit may be obtained
directly from ADC
®
, by calling our Customer Service Depart m e n t
toll-free at 1-800-ADC-2670 (p/n 991).
90 0 2
e - s p h y g TM 2
BLADDER
TUBE
Ca rea nd M ai n te na n ce
Other parts included depending upon model selected.

20 9
Pr eparation 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 corre c t l y.
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
b e f o re inserting the battery. Make sure " O" side of
MAIN POWER SWITCH is pressed down.
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)
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.
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.
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.
(Fig. 1)
(Fig. 2)
(Fig. 3)
ADA P TER
PLU G
BAT T ERYPLU G
Er ror Displays and Trou b le sh o ot in g
If you cannot get correct measurement with the methods above, do not tamper
with the internal mechanism. Contact your dealer. If the unit malfunctions,
re t u rn it to the dealer or an authorized service representative for serv i c i n g
according to the warranty. The manufacturer provides service data to qualified
dealers.
ERROR SYMBOL/SYMPTOM CA US E RE ME DY
Measurement result Blood pressure was taken in Measurement result is saved
cannot be recalled or “MANUAL” mode. only when it is taken in
is not stored. “AUTO” mode.
Measurement cannot be
Cuff inflation does Battery is exhausted. made when BATTERY MARK
not start. is displayed. Recharge the
battery.
AC INDICATOR is lit AC INDICATOR also indicates
even when 9002 is The battery is inserted. whether the battery is being
turned off. charged or it is not being
charged.
Difference in voltages
The column LCD is between AC ADAPTER and
dim or brightness is 9002 is operated with the battery lead to differences
not steady.the battery. in LCD brightness. This does
not indicate a functional
problem.

10 19
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 discharg e d .
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 disap-
pear. 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.
Er ror Displays and Trou bl e sh oo t in g
ERROR SYMBOL/SYMPTOM CA US E RE ME DY
LOW BATTERY: Change the battery. Only a
Battery is weak. few measurements can be
made before the battery
runs down.
BATTERY ERROR: Charge the battery.
Battery is exhausted. Measurement cannot be
conducted.
Turn off the device or press
ENERGY SAVER MODE: START/STOP button or
The device was left turned SET/MEMORY button to
on and has not been activate the device from
operated for over energy saving mode.
approximately 3 minutes. Make sure to turn off the
device by pressing “o” side
of MAIN POWER SWITCH
after use.
Measurement is When the preset pressureThis does not indicate a
interrupted once and value was not high enough to problem.
the cuff is inflated again. make measurement or when
noise was detected, the cuff
is pressurized again to a
higher level.
Patient moved during Make sure that the patient
measurement. stays still and quiet during
measurement.
Patient is not being measure d
Blood pressure is with correct posture. Make sure that
different each time. Blood pressure readings the patient is
The reading is extremely constantly vary with time being measured with
low (or high). of measurement and physical correct posture.
and mental condition.
Patient moved during Make sure that the patient
Pulse rate is too low measurement. There was not stays still during
(or too high). enough rest taken beforemeasurement. Allow your
measurement. patient to rest for at least
5 minutes.
The indication appearing
during LCD segment test,
which is performed when
the unit is turned on, does
not indicate low battery
or battery error.

18 11
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).
(Figur e 1)
2. Attach manometer to wall bracket by lowering atop 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 securel y with large (6mm)
allen wrench (Figure 2).
3. 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).
4. Attach 8 foot length coiled tubing to air inlet on face of
e-sphyg 2TM (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
Figure 3
Figure 6
Figure 4
Figure 1
Figure 5
How to Assemble Wall Model
Er ror Displays and Trou ble sh oot in g
ERRORSYMBOL/SYMPTOM CAUSE REMEDY
OVER-PRESSURIZATION: Make sure that
The cuff was inflated to the the patient
maximum pressure because stays still during
of movement of body, etc. measurement.
MEASUREMENT ERROR: Make sure the
Measurement could not be patient remains
made because of moving or still and quiet
talking during measurement. during measurement.
INFLATION ERROR: Reinsert AIR PLUG and make
AIR PLUG is not correctly sur e that it is securely inserte d.
inserted.
Make sure that the patient
Noise was detected. stays still and quiet during
measurement.
DEFLATION ERROR: Make sure the patient
Movement or talking was remains still and
detected during measurement. quiet during measurement.
Extreme changes in pressure Do not let patient move during
occurred during measurement. measurement.
CHECKING MODE: Turn off the device once and
See page 21. then turn it on again to take
measurement.
NO POWER: Reinsert AC ADAPTER and
AC ADAPTER is not make sure that it is securely
correctly connected. inserted.
Battery is exhausted. Charge the battery or use
AC ADAPTER.
Nothing is being Turn off the device or press
displayed when 9002 was left turned on but START/STOP button or
MAIN POWER SWITCH has not been operated for SET/MEMORY button
is pressed down in the over an hour.to activate the device
ON position. from energy saver mode.

12 517
1. With base on its side connect upright outer pole to base
using large (6mm) allen bolt. Tighten with large (6mm)
allen key p r ovided. Tighten hardware as securely as
p o s s i ble. (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 4
Figure 1
Figure 2
Figure 3
Figure 5

How to Assemble Mobile Model M e m o ry 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 perf o rmed
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.
Tu r n off the device by pressing "O" side of MAIN POWER SWITCH.
The device will be in the energy saver mode approximately after
3 minutes if it is not turned off. See page 10.

16 13
PLUG / PORT
CONNECTION
AIR CONNECTOR
(Coiled Tubing)
Cu ff Connections
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 f i rmly “lock” snaps
into the port(Figure 1).
2. Firmly insert male connector of coiled tubing into
female connector at end of the AdcuffT M bladder tubing.
Be sure the connectors are tight (Figure 2).
MALE
CONNECTOR
(Coiled Tubing)
FEMALE CONNECTOR
(Bladder Tube)
Figur e 2
F i g u re1
Taking Blood P re ssu re (Auto Mode)
Tu r n 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" measure m ent.
Set the initial inflation value with PRESET PRESSURE KNOB.
Select the pre s sure approximately 30 to 40 mmHg above
expected systolic pres s u re.
Pressure can be set between 100 mmHg and 280 mmHg.
Set the pres s u re at 180 mmHg if patient's systolic pre s s u re is
difficult to predict.
The cuff is re-pressurized to a higher value if the preset
pressu r e is too low for blood pressure to be taken during cuff
deflati o n .
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. Pres s u re does not exceed 290 mmHg.
Press START/STOP button when blood pre s s u re is taken and air
is rapidly exhausted from the cuff .
Air is also rapidly exhausted from the cuff when pre s s u re
descends to 30 mmHg.
Tu r n off the device by pressing "O" side of MAIN POWER SWITCH.
The device will be in the energy saver mode approximately after
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 measure m e n t .
Confir m that the cuff is kept at the height of patient's heart during measure m e nt.
Do not execute repeated measurements for congestion of blood could resul t
in false measurement. Allow the patient's arm to rest for at least 5 minutes.
Apply the cuff and stethoscope to the patient's arm in the same
manner as the usual auscultatory method.
Press STA RT/STOP button.
The cuff is inflated automatically after zero settings.
Pressurization stops when pres s ure reaches the preset pre s sure value and
pressu re starts to descend.
Deflation rate is displayed at the lower right corner of the segment LCD.
NOTE: Press STA RT/STOP button whenever the measure m ent
should be interrupted. The device will rapidly exhaust air from the cuff.

14 15
Taking Blood Pr ess ure (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.
Tu r n 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” measure m e n t.
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.
The set deflation rate re t urns to the default value (2.5) when the
device is turned off.
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.
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 art e ry.
Press the surface of the cuff to make sure that the hook and
loop adhesive fastens securel y.
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 pre ssure readings may resul t .
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 restri c t e d ,
preventing accurate measure m e n t .
ARM CIRCUMFERENCE CUFF SIZE
10.28 to 16.1 inches (26.1 to40.9 cm) ADULT
13.5 to 20.04 inches (34.3 to50.9 cm) LARGE ADULT
7.48 to 10.71 inches (19.0 to27.2 cm) CHILD
Press START/STOP button.
The cuff is inflated automatically after zero settings.
Pressurization stops when pre s sure reaches the preset pressure value and
pressu re 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 measurem e n t
should be interrup t e d .
The device will stop during any course of measurement
proced u re and rapidly exhaust air from the cuff.
Air is rapidly exhausted from the cuff as
measurement completes.
Blood pre s s u re and pulse rate are displayed.
Tu r n off the device by pressing "O" side of MAIN POWER SWITCH.
The device will go to the energy saver mode after approx i m ately
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 measuremen t
and refrains from talking or moving during measurement.
Confir m 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.