18
6 Miscellaneous
GB
• 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 com-
pletely 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.
• You are advised to store the unit in the storage case acquired upon purcha-
se and to keep it in a clean and dry place.
•
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.
Dispose of your old electrical unit in an environmentally acceptable manner
when it has reached the end of its service life!
Packaging is re-usable or may be re-cycled; metal parts must be disposed of
as scrap metal; plastics, electrical and electronic components must be disposed
of as electro-scrap.
Please remove the batteries before disposing of the equipment. Do not dis-
pose of old batteries with your household waste, but dispose of them at a
battery collection station at a recycling site or in a shop.
Consult your local council or your dealer for recycling information.
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 1060-
1/1995 and EN 1060-3/1997.
The specifications of EU Guideline “93/42/EEC of the Council Directive dated
14 June 1993 concerning medical devices” are met and likewise those of EU
Guideline 89/336/EEC.
Device classification:
type BF
User group:
The unit is suitable for non-invasive blood pressure measurements on adults
(this means that is it suitable for external use).
6.4
Disposal
6.5
Directives /
Norms
6.3
Care and
maintenance
Summary of Contents for MTA 51005
Page 95: ...91 GR 1 1 1 1 3 1 2 M MTA MEDISANA MEDISANA MTA S E 10...
Page 97: ...93 GR 2 2 4 WHO 2 5 2 6 WHO 100 100 140 60 60 90 1 2 3 140 159 160 179 180 90 95 110 5...
Page 98: ...94 3 GR 3 1 3 2 AA LR 6 Display MEDISANA 51008 1 1 2 3 12 2 MEMORY 3 4 2 5 MEMORY 6 0...
Page 100: ...96 4 5 GR 5 2 5 1 4 4 4 3 1 E 2 E 1 0 3 4 5 60 E 60 MEMORY MEMORY 60 MEMORY 5...
Page 101: ...97 GR 6 6 1 6 2 300 mmHg 1 5 V AA 300 mmHg 1 5 V AA...
Page 102: ...98 6 GR CE CE 0297 EN 1060 1 1995 EN 1060 3 1997 93 42 E 14 1993 89 336 E BF 6 4 6 5 6 3...
