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EMC GUIDANCE

EMC GUIDANCE

22

23

 

 

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 

Содержание TMB-1018-A

Страница 1: ...r selecting TRANSTEK Blood Pressure Monitor TMB 1018 A Please keep this manual well in order to reference in future Arm Type Version 1 0 EC REP Guangdong Transtek Medical Electronics Co Ltd Zone A No...

Страница 2: ...ON FOR USER 13 Tips for measurement Maintenances ABOUT BLOOD PRESSURE 15 What are systolic pressure and diastolic pressure What is the standard blood pressure classification Why does my blood pressure...

Страница 3: ...deflate Should the cuff not deflate when pressures exceeds 40 kPa 300 mmHg detach the cuff from the arm and press the START STOP button to stop inflation The equipment is not AP APG equipment and not...

Страница 4: ...ure 1kPa 7 5mmHg Low battery Batteries are low and need to be replaced Shocking reminding Shocking will result in inaccurate Average The average of blood pressure Recalling The records will be showed...

Страница 5: ...ery cover Install the batteries by matching the correct polarity as shown Replace the cover 1 Battery powered mode 6VDC 4 AAA batteries 2 AC adaptor powered mode 6V 1A Please only use the recommended...

Страница 6: ...he cuff should be snug but not too tight You should be able to insert one finger between the cuff and your arm 3 Sit comfortably with your tested arm resting on a flat surface 2 3cm 4 Repeat steps 2 a...

Страница 7: ...st CAUTION The order of the record date time will display alternately 1 When the monitor is off press the START STOP to turn on the monitor and it will finish the whole measurement Adjust the zero LCD...

Страница 8: ...3 If you don t want to delete the records press START STOP to escape If you did not get the correct measurement you can delete all results by following steps below Delete the Records 4 If there is no...

Страница 9: ...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 Th...

Страница 10: ...fer 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 AC adaptor is inserted incorrectly Inser...

Страница 11: ...00 240V 50 60Hz 400mA Output 6V 1A Type UE08WCP 060100SPA Conforms to UL certificate Contact Information For more information about our products please visit www transtek cn you can get customer servi...

Страница 12: ...ablishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Risk management Labeling User manual General Requirements for...

Страница 13: ...G 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 8...

Страница 14: ...the device as recommended below according to the maximum output power of the communications equipment Rated maximum output power of transmitter W Separation distance according to frequency of transmit...

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