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Duodynator
gbo Medizintechnik AG
Version 1.2
6.3
Safety checks
The device is subject to the provisions of the Medical Device Directive. The safety
controls have to be carried out on the basis of this directive. Thereby, the operator
regulation has to be observed in particular.
Irrespective of the legal rules or beyond the scope of the Medical Device Directive, it
is madatory to have the device checked at 12-months intervals by the manufacturer or
by a maintenance service authorized by him.
The review must consist at least of the following criteria:
Electrical safety check in accordance with the test plan of the manufacturer
Review of the device in respect of external integrity
Review of all display and operating elements in respect of damages
Review of all inscriptions in respect of immaculate legibility
Review of power supply cord and all patient connecting cables
Functional check
6.4
Disposal of equipment and accessories
According to the WEEE Directive 2002/96/EG (waste electrical and electronic
equipment) this device must not be disposed of with the domestic waste. The device
must be returned to the manufacturer for disposal. The manufacturer is committed to
guarantee the disposal of all devices marketed. This is also indicated by the WEEE
sign (crossed out waste container).