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EMC GUIDANCE

EMC GUIDANCE

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EMC Guidance

The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments.

Warning: Don’t be near the active HF surgical equipment and the RF shielded room of an ME 

system for magnetic resonance imaging, where the intensity of EM disturbances is high.

Warning: Use of this equipment adjacent to or stacked with other equipment should be avoided 

because it could result in improper operation. If such use is necessary, this equipment and the 

other equipment should be observed to verify that they are operating normally.

Warning: Use of accessories, transducers and cables other than those specified or provided by 

the manufacturer of this equipment could result in increased electromagnetic emissions or 

decreased electromagnetic immunity of this equipment and result in improper operation.

Warning: Portable RF communications equipment (including peripherals such as antenna 

cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of 

the equipment TMB-1491-BHJ including cables specified by the manufacturer. Otherwise, 

degradation of the performance of this equipment could result.

Technical description

1. All necessary instructions for maintaining BASIC SAFETY and ESSENTIAL 

PERFORMANCE with regard to electromagnetic disturbances for the excepted service life.

2. Guidance and manufacturer’s declaration-electromagnetic emissions and Immunity.

Table 1 

Guidance and manufacturer’s declaration - electromagnetic emissions

RF emissions

CISPR 11 

RF emissions

CISPR 11 

Group 1 

Class [ B ]

Class A

Comply

Compliance

Harmonic emissions

IEC 61000-3-2 

Voltage fluctuations / 

flicker emissions

IEC 61000-3-3

Emissions test

 

 

 

Table 2 

 

Guidance and manufacturer’s declaration – electromagnetic Immunity 

Immunity Test

 

±8 kV contact

±2 kV, ±4 kV, ±8 kV,  ±15 kV air 

±8 kV contact

±2 kV, ±4 kV, ±8 kV,  ±15 kV air 

 

±2 kV for power supply lines

±1 kV signal input/output 

100 kHz repetition frequency

±2 kV for power supply lines

Not Applicable

100 kHz repetition frequency

±0.5 kV, ±1 kV differential mode

±0.5 kV, ±1 kV, ±2 kV common mode    

±0.5 kV, ±1 kV differential mode

Not Applicable   

30 A/m

50 Hz / 60 Hz

30 A/m

50 Hz / 60 Hz

NOTE  U

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

Compliance level

Electrostatic

discharge (ESD) 

IEC 61000-4-2  

Power frequency 

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

IEC61000-4-5

IEC 60601-1-2 

Test level

0% U

T

; 0,5 cycle. At 0°, 45°, 90°, 135°,

180°, 225°, 270° and 315°.

0% U

T

; 1 cycle and 70% U

T

25/30 cycles; Single phase: at 0°.

0% U

T

; 250 / 300 cycle 

0% U

T

; 0,5 cycle. At 0°, 45°, 90°, 135°,

180°, 225°, 270° and 315°.

0% U

T

; 1 cycle and 70% U

T

25/30 cycles; Single phase: at 0°.

0% U

T

; 250 / 300 cycle 

Conduced RF

IEC61000-4-6

3 V

0,15 MHz – 80 MHz

6 V in ISM and amateur radio bands 

between 0,15 MHz and 80 MHz

80% AM at 1 kHz

3 V

0,15 MHz – 80 MHz

6 V in ISM and amateur radio bands 

between 0,15 MHz and 80 MHz

80% AM at 1 kHz

10 V/m

80 MHz – 2,7 GHz

80% AM at 1 kHz

10 V/m

80 MHz – 2,7 GHz

80% AM at 1 kHz

Radiated RF

IEC61000-4-3

Summary of Contents for TMB-1491-BHJ

Page 1: ...onitor Please read the user manual carefully and thoroughly so as to ensure the safe usage of this product Keep this manual for further reference in case any issues arise Version 1 0 Guangdong Transte...

Page 2: ...the Records Delete the Records INFORMATION FOR USER 21 Tips for measurement Maintenance ABOUT BLOOD PRESSURE 23 What are systolic pressure and diastolic pressure What is the standard blood pressure c...

Page 3: ...such as cardiac pacemakers de brillators Contraindications This product uses the Oscillometric Measuring method to detect blood pressure Before every measurement the unit establishes a zero pressure...

Page 4: ...f patient blood circulation When measurement please avoid compression or restriction of the connection tubing CAUTION The device cannot be used with HF surgical equipment at the same time The ACCOMPAN...

Page 5: ...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 prov...

Page 6: ...the measurement 6V 1A Do not use new and used ba eries together Do not use di erent types of ba eries together Do not dispose the ba eries in re Ba eries may explode or leak Remove ba eries if the dev...

Page 7: ...EM bu on will increase the number by one in a cycling manner When you get the right year press SET bu on to con rm the entry The screen will then show a blinking number represen ng the MONTH It is imp...

Page 8: ...between user 1 user 2 and USER G guest 1 Press SET bu on to ensure your choice it will show User ID and donE and then turn o 2 7 A er the UNIT is set the LCD will display donE rst then display all th...

Page 9: ...ment Sensi ve people including pregnant women pre eclamp c and those who implanted medical electronic instruments should avoid using the unit whenever possible Keep the monitor at least 20 cen meters...

Page 10: ...eep breaths Rest for 5 minutes before rst measuring Wait at least 3 minutes between measurements This allows your blood circula on to recover The pa ent must relax as much as possible and do not move...

Page 11: ...1 is shown rst Each new measurement is assigned to the rst 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 from the list 2 Each press M...

Page 12: ...can delete all results for the selected user by following steps Take User 1 for example If there is no record when you press MEM bu on to check the record the right display will be shown 3 Tips for Me...

Page 13: ...n indicates that a pulse irregularity consistent with an irregular heart beat was detected during measurement Usually this is NOT a cause for concern However if the symbol appears o en we recommend yo...

Page 14: ...during use please check the following points PROBLEM SYMPTOM CHECK THIS REMEDY No power Low batteries Error message Display will not light up Ba eries are exhausted Replace with new ba eries Insert th...

Page 15: ...ery Powered Mode Internally Powered ME Equipment AC Adapter Powered Mode Class II ME Equipment A temperature range of 5 C to 40 C A rela ve humidity range of 15 to 90 non condensing but not requiring...

Page 16: ...ses Bio compatibility ISO 10993 1 2018 Biological evaluation of medical devices Part 1 Evaluation and testing within a risk management process ISO 10993 5 2009 Biological evaluation of medical devices...

Page 17: ...anufacturer s declaration electromagnetic emissions RF emissions CISPR 11 RF emissions CISPR 11 Group 1 Class B Class A Comply Compliance Harmonic emissions IEC 61000 3 2 Voltage fluctuations flicker...

Page 18: ...3 Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communicati ons equipment Band MHz Modulation W Distance m IMMUNITY TEST LEVEL V m TETRA 400 Pulse modulation b 18 Hz GMRS 460 FRS 460...

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