Gima KD-5923 Andon Handleiding

Gima Bloeddrukmeter KD-5923 Andon

Lees hieronder de 📖 handleiding in het Nederlandse voor Gima KD-5923 Andon (2 pagina's) in de categorie Bloeddrukmeter. Deze handleiding was nuttig voor 40 personen en werd door 2 gebruikers gemiddeld met 4.5 sterren beoordeeld

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Pagina 1/2

Note:

2.1 The clock format could be set by user.

2.2 Table 1 instructs the conversion relations between 24 hour format and 12

hour format.

Table 1

3. Connecting the cuff to the monitor

Insert the cuff tubing connector into the socket in the left side of the monitor.

Make certain that the connector is completely inserted to avoid air leakage dur-

ing blood pressure measurements.

your arm. You should be able to insert one nger between your arm and the

cuff.

Note:

• Please refer to the cuff circumference range in “SPECIFICATIONS” to make

sure that the appropriate cuff is used.

• Measure on the same arm each time.

• Do not move your arm, body, or the monitor and do not move the rubber tube

during measurement.

• Stay quiet, calm for 5 minutes before blood pressure measurement.

• Please keep the cuff clean. If the cuff becomes dirty, remove it from the mon-

itor and clear it by hand in a mild detergent, then rinse it thoroughly in cold

water. Never dry the cuff in clothes dryer or iron it. Clean the cuff after the

usage of every 200 times is recommended.

• Do not place the cuff around your arm if the arm has any inammation, acute

diseases, infections skin wounds.

5. Body posture during measurement

Sitting Comfortably Measurement

a. Be seated with your feet at on the oor, and don’t

cross your legs.

b. Place palm upside in front of you on a at surface

such as a desk or table.

IMPORTANT INFORMATION .............................................................................3

CONTENTS AND DISPLAY INDICATORS .........................................................4

INTENDED USE .................................................................................................5

PACKAGE CONTENTS .....................................................................................5

CONTRAINDICATION ........................................................................................5

PRODUCT DESCRIPTION.................................................................................6

SPECIFICATIONS ..............................................................................................7

NOTICE .............................................................................................................8

SETUP AND OPERATING PROCEDURES ......................................................12

1. Battery loading ............................................................................................12

2. Clock and date adjustment .........................................................................13

3. Connecting the cuff to the monitor .............................................................15

4. Applying the cuff .........................................................................................16

5. Body posture during measurement .............................................................17

6. Taking your blood pressure reading ............................................................18

7. Displaying stored results .............................................................................19

8. Deleting measurements from the memory ..................................................21

9. Assessing high blood pressure for adults ...................................................22

10. Technical alarm description .......................................................................23

11. Troubleshooting (1) ....................................................................................24

12. Troubleshooting (2) ....................................................................................25

MAINTENANCE ...............................................................................................26

EXPLANATION OF SYMBOLS ON UNIT .........................................................28

ELECTROMAGNETIC COMPATIBILITY INFORMATION .................................30

WARRANTY INFORMATION ...........................................................................33

IMPORTANT INFORMATION

Normal blood pressure uctuation

All physical activity, excitement, stress, eating, drinking, smoking, body posture

and many other activities or factors (including taking a blood pressure measure-

ment) will inuence blood pressure value. Because of this, it is mostly unusual to

obtain identical multiple blood pressure readings.

Blood pressure uctuates continually day and night. The highest value usually

appears in the daytime and lowest one usually at midnight. Typically, the value

begins to increase at around 3:00AM, and reaches to highest level in the daytime

while most people are awake and active.

Considering the above information, it is recommended that you measure your

blood pressure at approximately the same time each day.

Too frequent measurements may cause injury due to blood ow interference,

please always relax a minimum moment of 1 to 1.5 minutes between measure-

ments to allow the blood circulation in your arm to recover. It is rare that you

obtain identical blood pressure readings each time.

7. Consult your physician if you have any doubt about below cases:

1) The application of the cuff over a wound or inammation diseases;

2) The application of the cuff on any limb where intravascular access or ther-

apy, or an arterio-venous (A-V) shunt, is present;

3) The application of the cuff on the arm on the side of a mastectomy or

lymph node clearance;

4) Simultaneously used with other monitoring medical equipments on the

same limb;

5) Need to check the blood circulation of the user.

8. This Electronic Sphygmomanometers is designed for adults and

should never be used on infants or young children. Consult your phy-

sician or other health care professionals before use on older children.

9. Do not use this unit in a moving vehicle, This may result in erroneous

measurement.

10. Blood pressure measurements determined by this monitor are equivalent to

those obtained by a trained observer using the cuff/stethoscope auscultation

method, within the limits prescribed by the American National Standard Insti-

tute, Electronic or automated sphygmomanometers.

11. Information regarding potential electromagnetic or other interference be-

tween the blood pressure monitor and other devices together with advice re-

garding avoidance of such interference please see part ELECTROMAGNET-

IC COMPATIBILITY INFORMATION. It is suggested that the blood pressure

monitor be kept at least 30 cm away from other wireless devices, such as

WLAN unit, microwave oven, etc.It can’t be used near active HF SURGICAL

EQUIPMENT and the RF shielded room of an ME SYSTEM for magneticres-

onance imaging, where the intensity of EM DISTURBANCES is high.

12. If Irregular Heartbeat (IHB) brought by common arrhythmias is detected in

the procedure of blood pressure measurement, a signal of will be dis-

played. Under this condition, the Electronic Sphygmomanometer can keep

function, but the results may not be accurate, it’s suggested that you consult

with your physician for accurate assessment.

There are 2 conditions under which the signal of IHB will be displayed:

1) The coefcient of variation (CV) of pulse period >25%.

2) The difference of adjacent pulse period≥0.14s, and the number of such

pulse takes more than 53 percentage of the total number of pulse.

13. Please do not use the cuff other than supplied by the manufacturer, other-

wise it may bring biocompatible hazard and might result in

measurement error.

14. The monitor might not meet its performance specications or cause

safety hazard if stored or used outside the specied temperature and

humidity ranges in specications.

15. Please do not share the cuff with other infective person to avoid

cross-infection.

16. This equipment has been tested and found to comply with the limits for a

Class B digital device, pursuant to part 15 of the FCC Rules. These limits

are designed to provide reasonable protection against harmful interference

in a residential installation. This equipment generates, uses and can radiate

CONTENTS AND DISPLAY INDICATORS

Note: The pictures in the manual are for reference only.

INTENDED USE

Fully Automatic Electronic Blood Pressure Monitor is for use by medical profes-

sionals or at home and is a non-invasive blood pressure measurement system

intended to measure the diastolic and systolic blood pressures and pulse rate of

an adult individual by using a non-invasive technique in which an inatable cuff is

wrapped around the upper arm. The cuff circumference is limited to 22cm-48cm

(approx. 8-18.2”).

PACKAGE CONTENTS

1 Blood Pressure Monitor

1 Operation Guide

1 Arm cuff 22-30cm (8-11’’)

1 Soft Storage Case

CONTRAINDICATION

It is inappropriate for people with serious arrhythmia to use this Electronic

Sphygmomanometer.

radio frequency energy and, if not installed and used in accordance with

the instructions, may cause harmful interference to radio communications.

However, there is no guarantee that interference will not occur in a particular

installation. If this equipment does cause harmful interference to radio or tel-

evision reception, which can be determined by turning the equipment off and

on, the user is encouraged to try to correct the interference by one or more

of the following measures:

- Reorient or relocate the receiving antenna.

- Increase the separation between the equipment and receiver.

- Connect the equipment into an outlet on a circuit different from that to

which the receiver is connected.

- Consult the dealer or an experienced radio/TV technician for help.

17. Measurements are not possible in patients with a high frequency of arrhyth-

mias.

18. The device is not intended for use on neonates, children or pregnant women.

(Clinical testing has not been conducted on neonates, children or pregnant

women.)

19. Motion, trembling, shivering may affect the measurement reading.

20. The device would not apply to the patients with poor peripheral circulation,

noticeably low blood pressure, or low body temperature (there will be low

blood ow to the measurement position).

21. The device would not apply to the patients who use an articial heart and

lung (there will be no pulse).

22. Consult your physician before using the device for any of the following con-

ditions: common arrhythmias such as atrial or ventricular premature beats or

atrial brillation, arterial sclerosis, poor perfusion, diabetes, pre-eclampsia,

renal diseases.

23. The patient is an intended operator.

24. Attention that changes or modication not expressly approved by the party

responsible for compliance could void the user’s authority to operate the

equipment.

25. Swallowing batteries and/or battery uid can be extremely dangerous. Keep

the batteries and the unit out of the reach of children and disabled persons.

26. If you are allergic to plastic/rubber, please don’t use this device.

SETUP AND OPERATING PROCEDURES

1. Battery loading

a. Open battery cover at the back of the monitor.

b. Load four “AAA” size batteries. Please pay attention to polarity.

c. Close the battery cover.

When LCD shows battery symbol , replace all batteries with new ones.

Rechargeable batteries are not suitable for this monitor.

Remove the batteries if the monitor will not be used for a month or more to avoid

relevant damage of battery leakage.

PRODUCT DESCRIPTION

Based on Oscillometric methodology and silicon integrated pressure sensor,

blood pressure and pulse rate can be measured automatically and non-invasive-

ly. The LCD display will show blood pressure and pulse rate. The most recent

4x30 measurements can be stored in the memory with date and time stamp.

The Electronic Sphygmomanometer corresponds to the below standards: IEC

60601-1Edition 3.1 2012-08/EN 60601-1:2006/A1:2013 (Medical electrical

equipment -- Part 1: General requirements for basic safety and essential perfor-

mance), IEC60601-1-2:2014/EN 60601-1-2:2015(Medical electrical equipment

-- Part 1-2: General requirements for basic safety and essential performance

- Collateral standard: Electromagnetic compatibility - Requirements and tests),

IEC80601-2-30:2009+AMD1:2013/EN IEC80601-2-30:2019 (Medical electrical

equipment –Part 2-30: Particular requirements for the basic safety and essential

performance of automated non-invasive sphygmomanometers)EN 1060-1: 1995

+ A2: 2009 (Non-invasive sphygmomanometers - Part 1: General requirements),

EN 1060-3: 1997 + A2: 2009 (Non-invasive sphygmomanometers - Part 3: Sup-

plementary requirements for electro-mechanical blood pressure measuring sys-

tems); ISO81060-2:2013(Non-Invasive Sphygmomanometers - Part 2: Clinical

Validation Of Automated Measurement Type).

13. Environmental humidity for operation: ≤85% RH

14. Environmental temperature for storage and transport:

-20°C~50°C (-4°F~122°F)

15. Environmental humidity for storage and transport: ≤85% RH

16. Environmental pressure: 80kPa-105kPa

17. Battery life: Approx 270 times.

18. All components belonging to the pressure measuring system, including ac-

cessories: Pump, Valve, LCD, Cuff, Sensor

Note: These specications are subject to change without notice.

NOTICE

1. Read all of the information in the operation guide and any other literature in

the box before operating the unit.

2. Stay quiet, calm and rest for 5 minutes before blood pressure measurement.

3. The cuff should be placed at the same level as your heart.

4. During measurement, neither speak nor move your body and arm.

5. Measuring on same arm for each measurement.

6. Please always relax a minimum moment of 1 to 1.5 minutes between meas-

urements to allow the blood circulation in your arm to recover.

Prolonged over-ination (cuff pressure exceed 300 mmHg or maintained

above15 mmHg for longer than 3 minutes) of the bladder may cause ecchy-

moma of your arm.

Avoid compression or restriction of the con-

nection tubing during measurement, which

may cause ination error, or harmful injury due

to continuous cuff pressure.

4. Applying the cuff

a. Pulling the cuff end through the medal loop (the

cuff is packaged like this already), turn it outward

(away from your body) and tighten it and close the

Velcro fastener. See picture 4-1.

b. Place the cuff around a bare left arm 1-2cm above

the elbow joint.

c. If you place the cuff around left arm,position the

air tube in the middle of your arm in line with your

middle nger. See picture 4-2.

If you place the cuff around right arm, apply the

cuff so that the air tube is at the side of your

elbow. See picture 4-3.

d. While seated, place palm upside in front of you on

a at surface such as a desk or table. Be careful

not to rest your arm on the air tube, or otherwise

restrict the ow of air to the cuff.

e. The cuff should t comfortably, yet snugly around

c. The middle of the cuff should be at the level of the right atrium of the heart.

Lying Down Measurement

a. Lie on your back.

b. Place your left arm straight along your side with

your palm upside.

c. The cuff should be placed at the same level as

your heart.

6. Taking your blood pressure reading

a. After applying the cuff and your body is in a comforta-

ble position, press the “START/STOP” button. All dis-

play characters are shown for self-test. You can check

the LCD display according to the right picture.

Please contact the service center if segment is missing.

b. Then the current memory bank ( , , or ) is displayed.

Press “MEM” button to change over to other bank.

Conrm your selection by pressing “START” button.

The current bank can also be conrmed automatically

after 5 seconds with no operation.

c. Then the monitor inates the cuff until sufcient pres-

sure has built up for a measurement. Then the monitor

slowly releases air from the cuff and carries out the

measurement.

the number will increase faster.

Picture 2-1 Picture 2-2 Picture 2-3

Picture 2-4 Picture 2-5 Picture 2-6

e. During adjusting clock and date, the monitor will go back to Standby Mode

automatically when no button will be pressed within 30 seconds.

f. You can turn off the monitor by pressing “START/STOP” button when the

minute is blinking, then the time and date is conrmed.

SPECIFICATIONS

1. Product name: Arm Blood Pressure Monitor

2. Model: 32901 / KD-5923

3. Classication: Internally powered, Type BF applied part, IP20, No AP or APG,

Continuous operation

4. Machine size: Approx. 107 mm × 80 mm × 52 mm

5. Cuff circumference: 22-30 cm (8-11”), 30-42 cm (11-16”) optional,

42-48 cm (16-18.2”) optional.

6. Weight: Approx. 166g (5 27/32 oz.) (exclude batteries and cuff)

7. Measuring method: oscillometric method, automatic air ination and meas-

urement

8. Memory volume: 4×30 times with time and date stamp

9. Power source: batteries: 4×1.5V SIZE AAA

10. Measurement range:

Cuff pressure: 0-300 mmHg

Systolic: 60-260 mmHg

Diastolic: 40-199 mmHg

Pulse rate: 40-180 beats/minute

11. Accuracy: Pressure: ±3 mmHg

Pulse rate: Less than 60: ±3bpm

More than 60 (incl.): ±5%

precision of the displayed values: 1mmHg

12. Environmental temperature for operation: 10°C~40°C (50°F~104°F)

Avoid the battery uid to get in your eyes. If it should get in your eyes, im-

mediately rinse with plenty of clean water and contact a physician.

The negative terminal of the battery needs to be compressed into the bat-

tery compartment properly after horizontal compression of the negative

electrode. The battery is in contact with the spring

Make sure the battery cover is intact and not damaged before installing

the battery.

The monitor, the batteries and the cuff, must be disposed of according to

local regulations at the end of their usage.

2. Clock and date adjustment

a. At rst the Blood Pressure Monitor is totally off, once you insert the battery,

the Blood Pressure Monitor will enter Clock and Date Adjustment Mode.

b. If the time of the device is already set and need to be changed, adjustment

can be reached by pressing both the “START/STOP” and “MEM” button for 3

seconds in Standby Mode.

c. In Clock and Date Adjustment Mode , the time format will blink at rst , see

picture2-1. The default time format is 24h and the default clock and date is

2016-1-1 1:00.

d. Press the button “START/STOP” repeatedly, the year (rst usage: default is

2016, range is 2016~2099), month, day, hour and minute will blink in turn, see

picture 2- 2& 2-3 & 2-4 & 2-5 & 2-6. While the number is blinking, press the

button “MEM” to increase the number, keep on pressing the button “MEM”,

ANDON VALUE DIGITAL

BLOOD PRESSURE MONITOR

Gima S.p.A.

Via Marconi, 1 - 20060 Gessate (MI) Italy

gima@gimaitaly.com - export@gimaitaly.com

www.gimaitaly.com

Operation Guide

24 hour format 12 hour format 24 hour format 12 hour format

0:00 12:00 AM 12:00 12:00 PM

1:00 1:00 AM 13:00 1:00 PM

2:00 2:00 AM 14:00 2:00 PM

3:00 3:00 AM 15:00 3:00 PM

4:00 4:00 AM 16:00 4:00 PM

5:00 5:00 AM 17:00 5:00 PM

6:00 6:00 AM 18:00 6:00 PM

7:00 7:00 AM 19:00 7:00 PM

8:00 8:00 AM 20:00 8:00 PM

9:00 9:00 AM 21:00 9:00 PM

10:00 10:00 AM 22:00 10:00 PM

11:00 11:00 AM 23:00 11:00 PM

Picture 4-1

Picture 4-2

Picture 4-3

PROFESSIONAL MEDICAL PRODUCTS

See picture 7-4.

Picture 7 Picture 7-1 Picture 7-2 Picture 7-3 Picture 7-4

c. Press “MEM” button again, LCD will display the average value of all the

results which is measured from 18 o’clock to 20 o’clock in last 7 days in

the current user memory zone. See picture 7-5. If no result stored from 18

o’clock to 20 o’clock in last 7 days, LCD will display “0” for blood pressure

and pulse rate. See picture 7-6.

Picture 7-5 Picture 7-6 Picture 7-7 Picture 7-8 Picture 7-9

d. Press “MEM” button again, the most recent result will be displayed with date

and time stamp. See picture 7-7. Irregular heartbeat symbol (if any) and blood

pressure classication indicator will blink at the same time. If the monitor has

no result stored in the current user memory zone, the LCD will display “0” for

blood pressure and pulse rate. See picture 7-8.

e. Press “MEM” button again to review the next result. See picture 7-9. In this

way, repeatedly pressing the “MEM” button displays the respective results

measured previously.

f. When reviewing the results, the monitor will turn off automatically after 1 min-

ute of no operation. You can also press the “START/STOP” button to turn off

the monitor manually.

Note: When the monitor displaying the measurement, the classication color

indicator can be shown different color according to the systolic pressure and

diastolic pressure. Refer to the “ASSESSING HIGH BLOOD PRESSURE FOR

ADULTS” section.

8. Deleting measurements from the memory

When any result is displaying, keeping on pressing but-

ton “MEM” for three seconds, all results will be deleted.

Press the button “START/STOP”, the monitor will turn off.

9. Assessing high blood pressure for adults

The following guidelines for assessing high blood pressure (without regard to

age or gender) have been established by the World Health Organization (WHO).

Please note that other factors (e.g. diabetes, obesity, smoking, etc.) need to be

taken into consideration. Consult with your physician for accurate assessment,

and never change your treatment by yourself.

Classication of blood pressure for adults

MAINTENANCE

1. Do not drop this monitor or subject it to strong impact.

2. Avoid high temperature and solarization. Do not immerse the monitor in

water as this will result in damage to the monitor.

Note: It is not intended to provide a basis of any type of rush toward emergency

conditions/diagnosis based on the color scheme and that the color scheme is

meant only to discriminate between the different levels of blood pressure.

10. Technical alarm description

The monitor will show ‘HI’ or ‘Lo’ as technical alarm on LCD with no delay if

the determined blood pressure (systolic or diastolic) is outside the rated range

specied in part SPECIFICACIONS. In this case, you should consult a physician

or check if your operation violated the instructions.

The technical alarm condition (outside the rated range) is preset in the factory

and cannot be adjusted or inactivated. This alarm condition is assigned as low

priority according to IEC 60601-1-8.

The technical alarm is non-latching and need no reset. The signal displayed on

LCD will disappear automatically after about 8 seconds.

12. Troubleshooting (2)

ELECTROMAGNETIC COMPATIBILITY INFORMATION

Table 1

Emission

12 It is recommended the cuff should be disinfected 2 times every week if need-

ed (For example, in hospital or clinic). Wipe the inner side (the side contacting

the skin) of the cuff with a soft cloth squeezed after being moistened with

Ethyl alcohol (75-90%), then dry the cuff by airing.

EXPLANATION OF SYMBOLS ON UNIT

Finally the blood pressure and pulse rate will be calculated and displayed

on the LCD screen. The blood pressure classication indicator and Irregular

heartbeat symbol (if any) will blink on the screen. The result will be automati-

cally stored in the monitor.

d. After measurement, the monitor will turn off automatically after 1 minute of no

operation.

e. During measurement, you can press the “START/STOP” button to turn off the

monitor manually.

Note: Please consult a health care professional for interpretation of pressure

measurements.

7. Displaying stored results

In StandBy Mode, press “MEM” button, the monitor will display sign of current

group. The amount of results in current user memory zone will be displayed. See

picture 7. Press “START/STOP” button to switch group,press “MEM” to conrm

current group. Then LCD will display the average value of all results in the current

user memory zone. See picture 7-1. If no result stored in the current user memory

zone, LCD will display “0” for blood pressure and pulse rate. See picture 7-2.

b. Press “MEM” button, LCD will display the average value of all the results

which is measured from 5 o’clock to 9 o’clock in last 7 days in the current

user memory zone. See picture 7-3. If no result stored from 5 o’clock to 9

o’clock in last 7 days, LCD will display “0” for blood pressure and pulse rate.

M32901-GB-Rev-2-02.20

32901 / KD-5923

PROBLEM POSSIBLE CAUSE SOLUTION

LCD shows

battery symbol

Low Battery Change the batteries

LCD shows “Er 0” Pressure system is unstable

before measurement

Don’t move and try

again

LCD shows “Er 1” Fail to detect systolic pressure

LCD shows “Er 2” Fail to detect diastolic

pressure

LCD shows “Er 3” Pneumatic system blocked or

cuff is too tight during ination

Apply the cuff correctly

and try again.

If the monitor is still ab-

normal, please contact

the local distributor or

the factory.

LCD shows “Er 4” Pneumatic system leakage

or cuff is too loose during

ination

LCD shows “Er 5” Cuff pressure above

300mmHg

Measure again after ve

minutes. If the monitor

is still abnormal, please

contact the local

distributor or the factory

LCD shows “Er 6” More than 3 minutes with cuff

pressure above 15 mmHg

LCD shows “Er 7” Inner memory error

LCD shows “Er 8” Device parameter checking

error

LCD shows “Er A” Pressure sensor parameter

error

No response when

you press button or

load battery

Incorrect operation or strong

electromagnetic interference

Take out batteries for

ve minutes, and then

reinstall all batteries

Table 2

Enclosure Port

Table 3

Proximity elds from RF wireless communications equipment

11. Troubleshooting (1)

PROBLEM POSSIBLE CAUSE SOLUTION

LCD Display shows

abnormal result

The cuff position was

not correct or it was not

properly tightened

Apply the cuff correctly

and try again

Body posture was not

correct during testing

Review the “BODY POSTURE

DURING MEASUREMENT”

sections of the instructions

and re-test

Speaking, arm or body

movement, angry, excited

or nervous during testing

Re-test when calm and

without speaking or moving

during the test

Irregular heartbeat

(arrhythmia)

It is inappropriate for people

with serious arrhythmia

to use this Electronic

Sphygmomanometer

Disposal: The product must not be disposed of along with other domestic

waste. The users must dispose of this equipment by bringing it to a specic

recycling point for electric and electronic equipment.

GIMA WARRANTY TERMS

The Gima 12-month standard B2B warranty applies.

WHO/ISH Denitions and classication of blood pressure levels

80 85 90 100 110

120

130

140

160

180

Severe Hypertension

Moderate Hypertension

Mild Hypertension

High-normal BP

Normal BP

Diastolic

(mmHg)

Systolic

(mmHg)

BLOOD PRESSURE

CLASSIFICATION

SBP

mmHg

DBP

mmHg

Color

Indicator

Optimal

<120 <80 green

Normal

120-129 80-84 green

High-Normal

130-139 85-89 green

Grade 1 Hypertension 140-159 90-99 yellow

Grade 2 Hypertension 160-179 100-109 orange

Grade 3 Hypertension ≥180 ≥110 red

Follow instructions for use

Caution: read instructions (warnings) carefully

Type BF applied part

WEEE disposal

0197

Medical Device complies with Directive

93/42/EEC

Manufacturer

Date of manufacture

Authorized representative in the European

community

Serial number

IP20 Covering Protection rate

Keep in a cool, dry place

Keep away from sunlight

Product code

Lot number

ANDON HEALTH CO., LTD.

No. 3 JinPing Street, Ya An Road, Nankai District,

Tianjin 300190, China

Made in China

iHealthLabs Europe SAS

36 Rue de Ponthieu,

75008, Paris, France

0197

IP20

Phenomenon Compliance Electromagnetic

environment

RF emissions CISPR 11 Group 1,

Class B

Home healthcare

environment

Harmonic distortion IEC 61000-3-2

Class A

Home healthcare

environment

Voltage uctuations

and icker

IEC 61000-3-3

Compliance

Home healthcare

environment

Phenomenon Basic EMC

standard

Immunity test levels

Home Healthcare

Environment

Electrostatic Discharge IEC 61000-4-2 ±8 kV contact

±2kV, ±4kV, ±8kV, ±15kV air

Radiated RF EM eld IEC 61000-4-3 10V/m

80MHz-2.7GHz

80% AM at 1kHz

Proximity elds from RF

wireless communications

equipment

IEC 61000-4-3 Refer to table 3

Rated power frequency

magnetic elds

IEC 61000-4-8 30A/m

50Hz or 60Hz

Test frequency

(MHz)

Band (MHz) Immunity test levels

Professional healthcare facility

environment

385 380-390 Pulse modulation 18Hz, 27V/m

450 430-470 FM, ±5kHz deviation, 1kHz sine,

28V/m

710 704-787 Pulse modulation 217Hz, 9V/m

745

780

810 800-960 Pulse modulation 18Hz, 28V/m

870

930

1720 1700-1990 Pulse modulation 217Hz, 28V/m

1845

1970

2450 2400-2570 Pulse modulation 217Hz, 28V/m

5240 5100-5800 Pulse modulation 217Hz, 9V/m

5500

5785

3. If this monitor is stored near freezing, allow it to acclimate to room tempera-

ture before use.

4. Do not attempt to disassemble this monitor.

5. It is recommended the performance should be checked every 2 years or after

repair. Please contact the service center.

6. Clean the monitor with a dry, soft cloth or a soft cloth squeezed well after

moistened with water, diluted disinfectant alcohol, or diluted detergent.

7. No component can be maintained by user in the monitor. The circuit dia-

grams, component part lists, descriptions, calibration instructions, or other

information which will assist the user’s appropriately qualied technical per-

sonnel to repair those parts of equipment which are designated repairably

can be supplied.

8. The monitor can maintain the safety and performance characteristics for a

minimum of 10,000 measurements or three years, and the cuff integrity is

maintained after 1,000 open–close cycles of the closure.

9. The monitor requires 6 hours to warm from the minimum storage tempera-

ture between uses until the monitor is ready for its INTENDED USE when the

ambient temperature is 20°C.

10. The monitor requires 6 hours to cool from the maximum storage temperature

between uses until the monitor is ready for its INTENDED USE when the

ambient temperature is 20°C.

11. Not servicing/maintenance while the monitor is in use.

Product specificaties

Merk:	Gima
Categorie:	Bloeddrukmeter
Model:	KD-5923 Andon

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