KaVo DIAGNOdent 2191, Инструкция по эксплуатации

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Instructions for use DIAGNOdent display 2191
2 Safety | 2.8 Disposal
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Have the service and testing tasks carried out according to the Medical
Device Operator Ordinance.
4 KaVo recommends specifying in-house service intervals where the medical
device is brought to a professional shop for cleaning, servicing and a func-
tion check. Define the service interval depending on the frequency of use.
A safety check is not required.
Operators, equipment managers and users in Germany are obliged to operate
their equipment in compliance with the medical device law ("MPG"). The main-
tenance services encompass all the test tasks required in accordance with § 6
of the operator ordinance ("MPBetreiberV").
As a result of the use of NON-KaVo original spare parts during the repair, parts
may become detached and injure patients, users or third parties. This may res-
ult in aspiration, swallowing of parts and possibly even a risk of suffocation.
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Only use spare parts that comply with the specification for repair; original
KaVo spare parts comply with the specification.
NOTE
If a repair is done with NON-KaVo original spare parts, this may constitute a
product modification that leads to the loss of CE conformity. In the event of
damage, the responsibility is with the service company or the operator.
The introduction of a modified product in the market, in which the reasonable
suspicion exists to endanger the safety and health of patients or users, is pro-
hibited by Medical Device Law §4, Abs.1 No. 1 and therefore requires its own
conformity check.
2.8 Disposal
This product is subject to the EC directive governing waste electrical and elec-
tronic devices and must be submitted to special disposal in Europe.
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For further information, please contact KaVo or a specialised dental dealer.