Information on electromagnetic compatibility
Note
Based on EN 60601-1-2 concerning the electromagnetic compatibility of electro‐
medical devices, we need to point out that:
• medical electrical devices are subject to special measures regarding electromag‐
netic compatibility and must be operated in accordance with KaVo assembly in‐
structions.
• portable and mobile high-frequency communications devices can influence med‐
ical electronics.
Note
KaVo cannot guarantee that accessories, lines and transformers not delivered by
KaVo will correspond with EMC requirements of EN 60601-1-2.
Disposal
Note
Any waste which is generated must be recycled or disposed of in a manner which
is safe both for people and for the environment. This must be done in strict com‐
pliance with all applicable national regulations.
Questions on proper disposal of the KaVo product can be answered by 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 accord‐
ingly within Europe.
Before disassembling / disposing of the product, it must be completely processed
(disinfected, sterilized) according to the section "Preparation methods"
Additional information can be obtained from KaVo (www.kavo.com) or your dental
supplier.
For final disposal, contact:
Instructions for use Globus 1078 S
2 Safety | 2.2 Purpose – Proper use
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Summary of Contents for Globus 1078 S
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