Care And Maintenance - ProMed MTX Instrucciones De Manejo

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 recalibrated 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 regu-
lations for users of medical equipment.
6.2 Disposal
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 dispose of old batteries with your household waste, but at a bat-
tery collection station at a recycling site or in a shop.
Consult your municipal authority or your dealer for information about disposal.
6.3 Guidelines / Standards
This blood pressure monitor meets the requirements of the EU standard for non-in-
vasive 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 medi-
cal 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 Miscellaneous
GB
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