Omron M24/7 instruction manual Technical Data, Technical parameters

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4. Technical Data

4.1. Technical parameters

Power supply:

2 AA rechargeable NiCd or NiMH batteries or 2 AA alkaline batteries

Display: liquid-crystal

Data storage:

internal solid state memory

Data transmission:

USB optical cable

PC interface:

USB interface

Operating environment:

Temperature: 10 - 45 °C

Humidity: 10 - 95 %, non condensing

Atmospheric pressure: 70 - 106 kPa

Storage conditions:

Temperature: -20 - 50 °C

Humidity: 10 - 95 %, non condensing

Size (H x W x D): 70 x 99 x 30 mm

Weight:

app. 240 g (batteries included)

Blood pressure measurement method: oscillometric

Blood pressure maximum storage: over 400 automatic measurements

Pressure measurement range: 0-300 mmHg

0-40 kPa*

Static accuracy:

±3 mmHg or 0,4 kPa or ± 2% of measured value (stability: 2 years)

Blood pressure measurement range indication:

30-260 mmHg

4-35 kPa*

Pulse rate measurement range: 40-200 beat per minute

Blood pressure measurement accuracy: The OMRON M24/7 has been clinically validated

Pressure sensor: piezo-resistive

In ation:

automatically controlled pump

Safety:

maximum in ation 300 mmHg (40 kPa*);

independent safety release valve

De ation and rapid air release: automatic pressure release valve

Please note that the OMRON M24/7 might not meet its performance speci cations if stored or used outside the speci ed environmental conditions.

*Measuring and LCD displaying in kPa values is an option which can be selected in the OMRON BP Tracker Software. The unit of measurement can be changed later in the database.

For information on cuffs and their application, see 2.8.

This symbol shows that according to regulations OMRON M24/7 should be handled as electronic waste during disposal.

Blood pressure measurements determined with the algorithm of an OMRON M24/7 monitor on adults are equivalent to those obtained by a trained observer using the cuff/stethoscope

￿by the American National Standard for Electronic or Automated Sphygmomanometers. The algorithm used in the OMRON M24/7 also ful ls the requirements of the British Hypertension Society

Validation Protocol for Automated Blood Pressure Measuring Devices.auscultation method Korotkoff phase V, within the limits prescribed

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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 Overview Main UnitArm Cuffs Front sidePackage Contents DisplayUsing the Buttons Cancel a blood pressure measurementOperating Instructions Working with the Omron M24/7 UnitSwitching the device off Switching the device onBattery voltage check LCD checkOverview Display Set by PCRules of Monitoring Monitoring Step by StepNot required to repeat with each session Preparation of Monitoring SessionEvaluation Start the Omron BP Tracker SoftwareManual Programming Programming OptionsMeasurement Timing Manual Programming Step by StepBatteries SoftwareCuffs and their application Care and Maintenance Handling Errors and ProblemsProtection, cleaning and washing Maintenance and Storage Conditions AccessoriesRegular checks, warranty, service Correct Disposal of this ProductTechnical Data Technical parametersSafety Concerns Electric shock hazard protectionBiocompatibility Hazardous materialsEMC Information Emission test Compliance Electromagnetic EnvironmentPage Recommended Separation =3.5/E Transmitter W Recommended separation distanceSeparation distance in function of the frequency Ambulatory Blood Pressure Monitoring Product Warranty Information Remarks