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EN 1060-4:2004 Non-invasive sphygmomanometers

-Part 4: Test procedures to determine the overall

system accuracy of automated non-invasive

sphygmomanometers

ISO 81060-2:2013 Non-invasive sphygmomanometers

-Part 2: Clinical validation of automated measurement type

EN 60601-1-6:2010/IEC 60601-1-6:2010+A1:2013

Medical electrical equipment - Part 1-6: General

requirements for basic safety and essential

performance - Collateral standard: Usability

EN 62366:2008/ IEC 62366-1:2015 Medical devices

-Application of usability engineering to medical devices

EN 62304:2006/AC: 2008 / IEC 62304:2006 Medical

device software - Software life-cycle processes

ISO 10993-1:2009 Biological evaluation of medical devices

-Part 1:Evaluation and testing within a risk

management process

ISO 10993-5:2009 Biological evaluation of medical devices

- Part 5: Tests for in vitro cytotoxicity

ISO 10993-10:2010 Biological evaluation of medical devices

- Part 10: Tests for irritation and skin sensitization

Clinical

investigation

Usability

processes

Bio

-compatibility

Complied Standards List

EMC Guidance

1)This product needs special precautions regarding EMC and needs

to be installed and put into service according to the EMC information

provided, and this unit can be affected by portable and mobile RF

communications equipment.

2)* Do not use a mobile phone or other devices that emit electromagnetic

fields, near the unit. This may result in incorrect operation of the unit. 

3)Caution: This unit has been thoroughly tested and inspected to

assure proper performance and operation!

4)* Caution: This machine should not be used adjacent to or stacked

with other equipment and that if adjacent or stacked use is necessary,

this machine should be observed to verify normal operation in the

configuration in which it will be used.

Table 1 

Guidance and manufacturer’s declaration

– electromagnetic emissions

RF emissions

CISPR 11

Group 1

Class B

Class A

Complies

Compliance

Harmonic

emissions

IEC 61000-3-2
Voltage

fluctuations/

flicker emissions

IEC 61000-3-3

 

RF emissions

CISPR 11

Emissions test

Electromagnetic environment

- guidance

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.

 

The device uses RF energy only

for its internal function. Therefore,

its RF emissions are very low and

are not likely to cause any

interference in nearby electronic

equipment.

The device is suitable for use in all

establishments, other than domestic

and those directly connected to the

public low-voltage power supply

network that supplies buildings used

for domestic purposes.

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EMC GUIDANCE

COMPLIED STANDARDS LIST

Summary of Contents for LIFEHOOD TMB-1775

Page 1: ...htly so as to ensure the safe usage of this product and keep the manual well for further reference in case you have problems Guangdong Transtek Medical Electronics Co Ltd Zone B No 105 Dongli Road Tor...

Page 2: ...Replacing the Batteries DATA MANAGEMENT 17 INFORMATION FOR USER 19 Setting Date Time Contraindications LCD Display Signal General Description Indications for Use Measurement Principle Start the Measur...

Page 3: ...pulse rate measurement and the result storage The design provides you with two years of reliable service Readings taken by the TMB 1775 are equivalent to those obtained by a trained observer using the...

Page 4: ...Systolic pressure High blood pressure Diastolic pressure Low blood pressure EXPLANATION mmHg Measurement Unit of the blood pressure Low battery Batteries are low and need to be replaced Current Time Y...

Page 5: ...22cm 42cm 3 4 AAA batteries Please use LIFEHOOD authorized cuff The size of the actual cuff please refer to the label on the attached cuff Component list of pressure measuring system 1 Cuff 2 Air pipe...

Page 6: ...ries In order to get the optimal performance and protect your monitor please use the correct batteries CAUTION Do not use new and used batteries together Do not use different types of batteries togeth...

Page 7: ...Press M button to change the Each press will increase the number by one in a cycling manner When the monitor is off hold pressing START STOP for 3 seconds to enter the mode for year setting 10 11 BEF...

Page 8: ...your left upper arm Do not place the arm cuff over thick clothes 2 Insert the air plug into the air jack securely 3 Wrap the arm cuff firmly in place around your left upper arm The bottom edge of the...

Page 9: ...t mmHg mmHg min How to Sit Correctly To take a measurement you need to be relaxed and comfortably seated under comfortable room temperature Avoid bathing drinking alcohol or caffeine smoking exercisin...

Page 10: ...instead 2 Press the START STOP button to turn the monitor off It will automatically turn off within 1 minute mmHg mmHg min 2 Press the M to get the record you want The current No is No 1 Five records...

Page 11: ...the selected user by following steps below Delete the Records 1 Hold pressing M button for 3 seconds when the monitor is in the memory recall mode the flash display dEL ALL will show mmHg mmHg min 2...

Page 12: ...ter clean it with a dry cloth in case Avoid dusty and unstable temperature environment Do not attempt to clean the reusable cuff with water and never immerse the cuff in water What is the standard blo...

Page 13: ...mend you seek medical advice Please note that the device does not replace a cardiac examination but serves to detect pulse irregularities at an early stage An irregular heartbeat is detected when a he...

Page 14: ...sure again Relax for a moment and then measure again The measurement process does not detect the pulse signal Loosen the clothing on the arm and then measure again Warning message Relax for a moment R...

Page 15: ...Mode of operation Continuous operation Degree of protection Protection against ingress of water Software Version A01 Approx 120 2mm 108 2mm 68 5mm 4 AAA batteries user manual IP21 It means the device...

Page 16: ...d in the user manual Otherwise the performance and lifetime of the device will be impacted and reduced CAUTION This device is intended for adult use in homes only The device is not suitable for use on...

Page 17: ...n the same limb which other monitoring ME equipment is applied around simultaneously because this could cause temporary loss of function of those simultaneously used monitoring ME equipment On the rar...

Page 18: ...roper results or serious danger Do not wash the cuff in a washing machine or dishwasher The service life of the cuff may vary by the frequency of washing skin condition and storage state The typical s...

Page 19: ...meters Part 3 Supplementary requirements for electro mechanical blood pressure measuring systems IEC 80601 2 30 2013 Medical electrical equipment Part 2 30 Particular requirements for the basic safety...

Page 20: ...d by portable and mobile RF communications equipment 2 Do not use a mobile phone or other devices that emit electromagnetic fields near the unit This may result in incorrect operation of the unit 3 Ca...

Page 21: ...rcial 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 Powe...

Page 22: ...itter manufacturer NOTE 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is af...

Page 23: ...c 5kHz deviation1kHzsine GMRS 460 FRS 460 LTE Band 13 17 Pulse modulation b 217Hz Pulse modulation b 18Hz Pulse modulation b 217Hz Pulse modulation b 217Hz Pulse modulation b 217Hz GSM 800 900 TETRA 8...

Page 24: ...he reduced minimum separation distance Minimum separation distances for higher IMMUNITY TEST LEVELS shall be calculated using the following equation Where P is the maximum power in W d is the minimum...

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