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Classification of Devices
Classification by type of protection against electric shock:
- Class II devices
Classification by degree of protection against electric shock:
- Applied part type B
Classification by sterilization or disinfection method allowed by the manufacturer:
- Refer to Sterilization.
Classification by mode of operation:
- Continuously operating device
Thank you for purchasing the EndoSequence II.
Read this Operation Manual carefully before use for operation instructions and maintenance
guidelines. Keep this Operation Manual for future reference.
Application
This product is a cordless handpiece used primarily for root canal enlargement.
User
Only qualified personal is allowed to use the unit only for dentistry.
Prohibition
Do not use this motor handpiece in an extremely bent root canal. Do not use this for implants
other than endodontic treatment or other dental treatment.
Guidance and manufacturer's declaration - electromagnetic emissions
The EndoSequence II is intended for use in the electromagnetic environment specified below. The
customer or the user of the EndoSequence II should assure that is used in such an environment.
Emissions test
Emissions test
Electromagnetic environment - guidance
RF emissions
CISPR11
RF emmissions
CISPR11
Harmonic emissions
IEC61000-3-2
Voltage fluctuations/
flicker emissions
IEC61000-3-3
Group 1
class B
class A
Complies
The EndoSequence II uses RF energy only for
its internal function. Therefore, its RF emissions
are very low and are not likely to cause any
interference in nearby electronic equipment.
The EndoSequence II is suitable for use in all
establishments, including domestic
estabilishments and those directly connected
to the public low-voltage power supply
network that supplynetwork that spplies
buidings used for domestic purposes.
Содержание EndoSequence II
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