Omron M24/7 instruction manual

Page 23

Directive and declaration of manufacturer – Electromagnetic immunity

OMRON M24/7 is suitable for use in the speci ed electromagnetic environment. The purchaser or user of OMRON M24/7 should assure that it is used in an electromagnetic environment as described below.

Immunity test

IEC60601-1-2

Compliance

Electromagnetic

 

test level

level

environment

Electrostatic

±6KV contact

±8KV air

Floors are wood, concrete or

discharge (ESD)

±8KV air

 

ceramic tile, or oors are covered

IEC 61000-4-2

 

with synthetic material and the

 

 

 

 

relative humidity is at least 30

 

 

 

 

 

 

percent.

Electrical fast

±2KV for power

Not applicable

Mains power quality is that of a

transient/burst

supply lines

 

typical commercial and/or hospital

IEC 61000-4-4

±1KV for input/

 

environment.

 

 

 

output lines

 

 

Surge

±1KV differential

Not applicable

Mains power quality is that of a

IEC 61000-4-5

mode

 

typical commercial and/or hospital

±2KV common

 

environment.

 

 

 

 

 

 

mode

 

 

Voltage dips, short

<5% UT (>95%

Not applicable

Mains power quality is that of

interruptions and

dip) for 0.5 cycle;

 

a typical commercial and/or

voltage variations

40% UT (60% dip)

 

hospital environment. If the user of

on power supply

 

OMRON M24/7 requires CLINICAL

for 5 cycles;

 

input lines

 

UTILITY during power mains

70% UT (30% dip)

 

IEC 61000-4-11

 

interruptions, it is recommended

for 25 cycles;

 

that parts of the OMRON M24/7

 

 

 

<5% UT (>95%

 

system where applicable be

 

 

powered from an uninterruptible

 

dip) for 5 sec.

 

 

 

power supply.

 

 

 

Power frequency

3A/m

3A/m

Power frequency magnetic elds

(50/60Hz) magnetic

 

 

are at levels characteristic of

eld

 

 

a typical location in a typical

IEC 61000-4-8

 

 

commercial and/or hospital

 

 

environment.

 

 

 

Note: UT is the nominal voltage of mains.

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Contents M24/7 Ambulatory Blood Pressure Monitor Introduction Content Important Safety Information Important Safety InformationDamage to the equipment or other property Contraindications Recommended use of ambulatory blood pressure monitoringIndications Front side OverviewMain Unit Arm CuffsDisplay Package ContentsWorking with the Omron M24/7 Unit Using the ButtonsCancel a blood pressure measurement Operating InstructionsLCD check Switching the device offSwitching the device on Battery voltage checkSet by PC Overview DisplayMonitoring Step by Step Rules of MonitoringStart the Omron BP Tracker Software Not required to repeat with each sessionPreparation of Monitoring Session EvaluationManual Programming Step by Step Manual ProgrammingProgramming Options Measurement TimingSoftware BatteriesCuffs and their application Handling Errors and Problems Care and MaintenanceProtection, cleaning and washing Correct Disposal of this Product Maintenance and Storage ConditionsAccessories Regular checks, warranty, serviceTechnical parameters Technical DataHazardous materials Safety ConcernsElectric shock hazard protection BiocompatibilityEmission test Compliance Electromagnetic Environment EMC InformationPage Recommended Separation =3.5/E Transmitter W Recommended separation distanceSeparation distance in function of the frequency Ambulatory Blood Pressure Monitoring Product Warranty Information Remarks