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Guidance and manufacturer’s declaration – electromagnetic immunity 

IMMUNITY test

 

±6 kV contact
±8 kV air 

±6 kV contact
±8 kV air 

 

±2 kV for 
power supply lines 

Not applicable

±1 kV line(s) 
to line(s)
±2 kV line(s)

to earth 

<5% U

T

(>95% dip in U

T

)

for 0.5 cycle
40% U

T

(60% dip in U

T

)

for 5 cycles

70% U

T

(30% dip in U

T

)

for 25 cycles

<5% U

T

(>95% dip in U

T

)

for 5 s

3A/m

NOTE      U

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

Table 2 Guidance and MANUFACTURER’s declaration – electromagnetic 

IMMUNITY – for all ME EQUIPMENT and ME SYSTEMS 

IEC 60601 test level       Compliance level

Electrostatic 
discharge (ESD) 
IEC 61000-4-2 

Electromagnetic 

environment - guidance

Floors should be wood, 

concrete or ceramic tile. If 

floors are covered with 

synthetic material, the 

relative humidity should be 

at least 30%.

Power frequency magnetic 

fields should be at levels 

characteristic of a typical

location in a typical 

commercial or hospital 

environment.

3A/m

Power frequency 

(50/60Hz) 

magnetic field 

IEC 61000-4-8 

Voltage dips, 

short interruptions

and voltage

variations on 

power supply 

input lines

IEC 61000-4-11 

Electrical fast 
transient/burst 
IEC 61000-4-4 

Surge IEC 
61000-4-5

The device is intended for use in the electromagnetic environment specified below.

The customer or the user of the device should assure that it is used in such an

environment

±1 kV for 

input/output lines

Not applicable

Not applicable

Mains power quality should

be that of a typical

commercial or hospital

environment.

Mains power quality should

be that of a typical

commercial or hospital

environment.

Mains power quality should

be that of a typical

commercial or hospital

environment. If the user of

the device requires 

continued operation during

power mains interruptions,

it is recommended that the

device be powered from an

uninterruptible power supply

or a battery.

Table 4 Guidance and MANUFACTURER’s declaration – electromagnetic IMMUNITY –

for ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING 

Guidance and manufacturer’s declaration – electromagnetic immunity

IMMUNITY test

Not applicable

3 V/m 

Compliance 

level

IEC 60601 

TEST LEVEL

Conducted RF

IEC 61000-4-6 

Radiated RF 

IEC 61000-4-3

3 V/m

80 MHz to

2.5 GHz 

3 Vrms

150 kHz to

80 MHz 

Electromagnetic environment - 

guidance

Portable and mobile RF communications 

equipment should be used no closer to 

any part of the device, including 

cables, than the recommended 

separation distance calculated from the 

equation applicable to the frequency of 

the transmitter.

Recommended separation distance

The device is intended for use in the electromagnetic environment specified below.

The customer or the user of the device should assure that it is used in such an environment.

where

 P

 is the maximum output power

rating of the transmitter in watts (W) 

according to the transmitter manufacturer

and 

d

 is the recommended separation

distance in metres (m).

Field strengths from fixed RF 

transmitters, as determined by an 

electromagnetic site survey,   should be

less than the compliance level in each

frequency range.

a

b

Interference may occur in the vicinity of 

equipment marked with the following 

symbol:

P

=

d

P

=

d

 80 MHz to 800 MHz 

P

=

d

2,3

  800 MHz to 2,5 GHz 

1,2 

NOTE 1 

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

NOTE 2 

These guidelines may not apply in all situations. Electromagnetic 

                    propagation is affected by absorption and reflection from structures, objects

                    and people.

a

Field strengths from fixed transmitters, such as base stations for radio (cellular / cordless) telephones 

and land mobile radios, amateur radio, AM and FM radio broad-cast 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 device is used exceeds the applicable RF compliance level above, the 

device should be observed to verify normal operation. If abnormal performance is observed, 

additional measures may be necessary, such as re-orienting or relocating the device.

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

b

1,2 

27

26

EMC GUIDANCE

EMC GUIDANCE

Содержание TMB-1491

Страница 1: ...tor TMB 1491 Please do read the user manual carefully and thoroughtly so as to ensure the safe usage of this product and keep the manual well for further reference in case you have problems EC REP Guangdong Transtek Medical Electronics Co Ltd Zone A No 105 Dongli Road Torch Development District Zhongshan 528437 Guangdong China ...

Страница 2: ...he Records Delete the Records INFORMATION FOR USER 17 Tips for measurement Maintenances ABOUT BLOOD PRESSURE 19 What are systolic pressure and diastolic pressure What is the standard blood pressure classification Irregular heartbeat detector Why does my blood pressure fluctuate throughout the day Why do I get a different blood pressure at home compared to the hospital Is the result the same if mea...

Страница 3: ...ained observer using the cuff and stethoscope auscultation method This manual contains important safety and care information and provides step by step instructions for using the product Read the manual thoroughly before using the product Features 60mm 40 5 mm Digital LCD Maximum 60 records per each user General Description 3rd technology Measuring during inflation The updated technology in the wor...

Страница 4: ...unit is not suitable for continuous monitoring during medical emergencies or operations Otherwise the patient s arm and fingers will become anaesthetic swollen and even purple due to a lack of blood When not in use store the device in a dry room and protect it against extreme moisture heat lint dust and direct sunlight Never place any heavy objects on the storage case This device may be used only ...

Страница 5: ...ween uses until it is ready for intended use At least 30 min required for ME equipment to cool from the maximum storage temperature between uses until it is ready for intended use This equipment needs to be installed and put into service in accordance with the information provided in the ACCOMPANYING DOCUMENTS Wireless communications equipment such as wireless home network devices mobile phones co...

Страница 6: ...e display is dim The display does not light up Always select the authorized specified battery Four AAA size alkaline batteries Please use TRANSTEK authorized cuff The size of the actual cuff please refer to the label on the attached cuff Do not use new and used batteries together Do not use different types of batteries together Do not dispose the batteries in fire Batteries may explode or leak Rem...

Страница 7: ...tton shortly it will display the time Then hold pressing SET button to enter the mode for year setting 2 Press MEM button to to change the YEAR Each press will increase the numeral by one in a cycling manner 3 When you get the right year press SET button to set down and turn to next step 4 Repeat steps 2 and 3 to set the MONTH and DAY 5 Repeat steps 2 and 3 to set the HOUR and MINUTE 7 After the u...

Страница 8: ...art Turn your palm upwards Sit upright in a chair and take 5 6 deep breaths Rest for 5 minutes before first measuring Wait at least 3 minutes between measurements This allows your blood circulation to recover The patient must relax as much as possible and do not move and talk during the measurement procedure For a meaningful comparison try to measure under similar conditions For example take daily...

Страница 9: ... measurement is assigned to the first 1 record All other records are pushed back one digit e g 2 becomes 3 and so on and the last record 60 is dropped The current No is No 2 The corresponding time is A M 8 18 The corresponding date is January 1st CAUTION DOWN UP The date and time of the record will be shown alternately Note If you want to check another user s records please turn off the blood pres...

Страница 10: ...following circumstances If you did not get the correct measurement you can delete all results by following steps below Delete the Records 2 Press SET to confirm deleting and the monitor will turn off 3 If you don t want to delete the records press START STOP to escape 4 If there is no record the right display will show START STOP 1 Hold pressing MEM and SET for 3 seconds when the monitor is in the...

Страница 11: ...c pressure What is the standard blood pressure classification The blood pressure classification published by World Health Organization WHO and International Society of Hypertension ISH in 1999 is as follows Irregular Heartbeat Detector CAUTION The appearance of the IHB icon indicates that a pulse irregularity consistent with an irregular heart beat was detected during measurement Usually this is N...

Страница 12: ...ailer or our customer service department for further assistance Refer to the warranty for contact information and return instructions E21 shows The treatment of the measurement failed Relax for a moment and then measure again The monitor detected motion talking or the pluse is too poor while measuring Relax for a moment and then measure again 1 Individual blood pressure varies multiple times every...

Страница 13: ...bout our products please visit www transtek cn you can get customer service usual problems and customer download transtek will serve you anytime Authorized European Representative Manufactured by Company Address Company MDSS Medical Device Safety Service GmbH Address Schiffgraben 41 30175 Hannover Germany Guangdong Transtek Medical Electronics Co Ltd Zone A No 105 Dongli Road Torch Development Dis...

Страница 14: ...g and information to be supplied Part 1 General requirements IEC 80601 2 30 2013 Medical electrical equipment Part 2 30 Particular requirements for the basic safety and essential performance of automated non invasive sphygmomanometers ISO 81060 2 2013 Non invasive sphygmomanometers Part 2 Clinical validation of automated measurement type EN 60601 1 2 2007 IEC 60601 1 2 2007 Medical electrical equi...

Страница 15: ...eclaration electromagnetic immunity IMMUNITY test Not applicable 3 V m Compliance level IEC 60601 TEST LEVEL Conducted RF IEC 61000 4 6 Radiated RF IEC 61000 4 3 3 V m 80 MHz to 2 5 GHz 3 Vrms 150 kHz to 80 MHz Electromagnetic environment guidance Portable and mobile RF communications equipment should be used no closer to any part of the device including cables than the recommended separation dist...

Страница 16: ...ecommended below according to the maximum output power of the communications equipment Rated maximum output power of transmitter W Separation distance according to frequency of transmitter m For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres m can be estimated using the equation applicable to the frequency of the transmitter where P is...

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