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Instructions for use EXTRAmatic 9040
2 Safety | 2.2 Purpose – Intended use
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The following persons are authorised to repair and service the KaVo product:
▪ Technicians of KaVo branch offices after appropriate product training.
▪ Specifically KaVo-trained technicians of KaVo franchised dealers.
The applicable national legal regulations must be observed during the use of the de‐
vice, in particular the following:
▪ Applicable regulations governing the connection and start-up of medical devices.
▪ Current occupational safety regulations.
▪ Current accident prevention regulations.
Note
Any waste which is generated must be recycled or disposed of in strict compliance
with all applicable national regulations in a manner which is safe both for people
and the environment.
If you have any questions regarding proper disposal of the KaVo product, please
contact the KaVo branch.
Disposal of electronic and electrical devices
Note
According to EC directive 2002/96 concerning used electrical and electronic devi‐
ces, this product is subject to the cited directive and must be disposed of according‐
ly within Europe.
For more information, please visit www.kavo.com or contact your specialised dental
supplier.
For final disposal, please contact:
In Germany
To return an electrical device, you need to proceed as follows:
1. On the homepage www.enretec.de of enretec GmbH, you can download a form for
a disposal order under the menu item eom. Download the disposal order or com‐
plete it as an online order.
2. Enter the corresponding information to complete the order, and submit it as an on‐
line order or by fax +49 (0) 3304 3919-590 to enretec GmbH.
The following contact options are also available for questions and for initiating a
disposal order:
Phone: +49 (0) 3304 3919-500
Email: [email protected] and
Postal address: enretec GmbH, Geschäftsbereich eomRECYCLING®
Kanalstraße 17
D-16727 Velten
3. A unit that is not permanently installed will be picked up at the office.
A permanently installed unit will be picked up at the curb at your address on the
agreed date.
The owner or user of the device will have to bear the cost of disassembly, trans‐
portation and packaging.
International
For country-specific information on disposal, contact your dental supplier.
2.2.2 Product-specific
Restrictions on use:
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