Idiomas disponibles
Idiomas disponibles
28
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 specification lists all required test steps and the neces-
sary equipment.
Disposal
Reocor D is marked with the symbol of a crossed-out gar-
bage can on its type plate. The symbol indicates that the
European guideline 2002/96/EC on waste electrical and elec-
tronic 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
disposed 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.
