9–2 SCALER SETTINGS
9–2–1 [1. Version] : Display product information.
1.Version
DISPOSING PRODUCT
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In order to avoid the health risks of operators handling the disposal of medical equipment, as well as the risks
of environmental contamination caused thereof, a surgeon or a dentist is required to confirm the equipment is
sterile. Ask specialist firms who are licensed to dispose of specially controlled industrial wastes, to dispose the
product for you.
WARRANTY
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Manufacture warrants this product to the Original purchaser against defects in material and workmanship under
normal practices of installation, use and servicing. Article of consumption (such as O–Rings) is not covered by
this warranty.
Symbols
Type B applied part.
Follow the waste of electric and electronic equipment (WEEE) Directive (2012/19/EU) to dispose of the
product and accessories.
This conforms to CE European Directive of "Medical equipment directive 93/42/EEC."
Protected against vertically falling water drops.
Guidance and manufacturer's declaration – electromagnetic emissions
The Multi Pad is intended for use in the electromagnetic environment specified below. The customer or the user of the Multi Pad should assure
that is used in such an environment.
Emissions test
RF emissions
EN 55011
CISPR 11
RF emissions
EN 55011
CISPR 11
Harmonic emissions
EN 61000-3-2
IEC 61000-3-2
EN 61000-3-3
IEC 61000-3-3
LCD XXXX
VA170 XXXX
In case of iMD
NLX XXXX
iMD XXXX
Refer to Operation Manual.
Compliance
Electromagnetic environment – guidance
The Multi Pad uses RF energy only for its internal function. Therefore, its RF
Group 1
emissions are very low and are not likely to cause any interference in nearby
electronic equipment.
The Multi Pad is suitable for use in all establishments, including domestic
Class B
establishments and those directly connected to the public low–voltage power
supply network that supplies buildings used for domestic purposes.
Class A
Complies
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Manufacturer.