Bedienungsanleitung Medisana MTX 51080 bovenarm (Seite 42 von 182) (Deutsch, Englisch, Holländisch, Französisch, Italienisch, Portugiesisch, Spanisch, Schwedisch, Finnisch)

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6 Miscellaneous

6.1

Care and

maintenance

• Remove the batteries before cleaning the unit.

• Never use strong detergents or hard brushes.

• Clean the unit with a soft cloth, moistened with mild soapy water. Do not let

water enter the unit. After cleaning, only use the unit when completely dry.

• Remove the batteries from the unit if you do not wish to use it for an

extended period of time, otherwise there is a risk of battery leakage.

• Do not expose the unit to direct sunlight, and protect it from dust and

moisture.

• Only inflate the cuff when it is in position around the upper arm.

• Servicing and calibration

The unit has been calibrated by the manufacturer for a period of two years’

use. In the case of commercial use, the unit must be serviced and recali-

brated at least once every two years. This calibration will be charged for and

can be carried out by an appropriate authority or an authorised service

centre - in accordance with the regulations for users of medical equipment.

This product must not be disposed of together with domestic waste.

All users are obliged to hand in all electrical or electronic devices, regardless

of whether or not they contain toxic substances, at a municipal or commer-

cial collection point so that they can be disposed of in an environmentally

acceptable manner.

Please remove the batteries before disposing of the device / unit. Do not dis-

pose of old batteries with your household waste, but at a battery collection

station at a recycling site or in a shop.

Consult your municipal authority or your dealer for information about disposal.

This blood pressure monitor meets the requirements of the EU standard for

non-invasive blood pressure monitors. It is certified in accordance with EC

Guidelines and carries the CE symbol (conformity symbol) “CE 0297”.

The blood pressure monitor corresponds to European standards EN 60601-1,

EN 60601-1-2, EN 1060-1/-3/-4, EN ISO 14971 and EN 980.

The specifications of EU Guideline “93/42/EEC of the Council Directive dated

14 June 1993 concerning medical devices” are met.

Clinical trial results:

Clinical trials for this unit were carried out in the USA and Germany according

to EN 1060-4 and according to the AAMI – Standard (US).

Electromagnetic compatibility:

The device complies with the EN 60601-1-2 standard for electromagnetic

compatibility.

Inquire at MEDISANA for details on this measurement data.

Intended use:

This unit is suitable for non-invasive blood pressure measurement in adults

(i.e., suitable for external use).

6.2

Disposal

6.3

Guidelines /

Standards

51080_MTX_West_FINAL_akt.qxd:Blutdruckmessgerät 10.09.2009 11:16 Uhr Seite 32

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