Information On Electromagnetic Compatibility - KaVo INTRAsurg 300 Instructions For Use Manual

Surgical implant rotary system non optic unit
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Instructions for use INTRAsurg 300 / INTRAsurg 300 plus
2 Safety | 2.2 Purpose – Proper use
Note
The product must be cleaned and serviced according to instructions if it is not to
be used for a long period.
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.
Note
A recycling pass can be downloaded from www.kavo.com.

2.2.1 Information on electromagnetic compatibility

Conformance level: The immunity test levels required in IEC 60601 are met.
CAUTION
Damage from incorrect accessories
The use of other accessories, transformers and lines than those indicated (with the
exception of transformers and lines that KaVo sells as replacement parts for in‐
ternal components) can increase transmission or reduce the electromagnetic im‐
munity of the product.
▶ Only use accessories recommended by KaVo.
CAUTION
Interactions between devices
Effect on proper use
▶ Do not use the device directly next to or stacked with other devices
▶ If it is necessary to use it next to or stacked with other devices, check for proper
use in this set up.
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.
9/66

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Intrasurg 300 plus

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