Disposal - BIOTRONIK Reocor S Manual Tecnico

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Function test:
The result of the self-test that runs automatically after
activation must be heeded.
Inspection Inspections should be performed:
• after an application together with high-frequency surgi-
cal instruments or defibrillators,
• when malfunctions are suspected,
• once a year.
The inspection should follow the manufacturer specifica-
tions. These are made available upon request. The specifica-
tion lists all required test steps and the necessary equipment.

Disposal

Reocor S is marked with the symbol of a crossed-out garbage
can on its type plate. The symbol indicates that the European
guideline 2002/96/EC on waste electrical and electronic
equipment (WEEE directive) applies to the disposal method of
the device.
Old devices and accessories that are no longer needed,
such as patient cables and adapters, should be returned to
BIOTRONIK. This ensures that proper disposal will be carried
out in accordance with the national implementations of the
WEEE directive.
Note: Cables to be disposed of due to contact with blood must be
disposed of as medical waste, in accordance with environ-
mental regulations. Non-contaminated cables must be dis-
posed of in accordance with the European Directive 2002/96/
EC regarding waste electrical and electronic equipment
(WEEE).
Depleted batteries must be treated as hazardous waste and
disposed of by the user.
If you have any questions, please contact BIOTRONIK.