Cable Length; Disposal And Recycling; Manufacturer's Liability; Regulations - Ultradent Products Genius Manual Del Usuario

With regards to transmitters for which the maximum power is not listed above, the recommended separation distance (d) in
metres (m) can be estimated by using the equation applicable to the transmitter frequency where (P) is the maximum power
Note 1: At 80 MHz and 800 MHz, the highest frequency range applies.
Note 2: These specifications cannot be applied to all situations.
The electromagnetic propagation is reduced by the absorption and reflection of structures, objects and people.

10.5 CABLE LENGTH

Cables and Accessories
Handpiece cord
Control pedal cord
Power cord
XI - DISPOSAL AND RECYCLING
As an item of Electrical and Electronic Equipment, the medical device must be disposed of via a specialist collection, removal,
recycling or destruction channel. This applies in particular to the European market, in reference to Directive 2002/96/EC dated
27/01/2003.
When your device has reached the end of its life, we recommend contacting your dental equipment dealer or Ultradent to learn
how to proceed.
XII - MANUFACTURER'S LIABILITY
The manufacturer will not be held liable due to:
- failure to comply with the manufacturer's installation recommendations (grid voltage, electromagnetic environment,
etc.)
- servicing, changes, or repairs carried out by individuals not authorized by the manufacturer
- operation within an electrical setting not complying with applicable regulations
- uses other than those specified in this manual
- using accessories (motor and cord, pedal, etc.) other than those supplied by the distributor and manufacturer.
- failure to comply with the guidelines contained in this document
Note:
The manufacturer reserves the right to change the device and/or operating manual without notice.
XIII - REGULATIONS
This medical device is classified IIa under European directive 93/42/EEC. This equipment is manufactured in accordance with
the following standard: IEC 60601-1. This equipment was designed and manufactured according to EN ISO 13485 certified quality
assurance system.
XIV - SYMBOLS
This operating and maintenance manual provides instructions for the Genius
used are intended to help the end user understand functions and operations.
Target audience: Dentists and dental office staff.
Please keep this manual with the device so that it can be consulted at any time. If the device is sold or transferred to another
end user, please attach this manual to the device. The new end user will thus have all the information needed to understand
the functions of the device, and its proper use. These instructions are intended to ensure safe use of the equipment. Please
read them attentively before installing and using the device.
Description of safety instructions
Important information or explanations intended for users.
Direct impact on product function or warning of improper and/or potentially hazardous use for product or operator.
Three hazard levels are used in this document to avoid any damage to the device and personal injury.
14
Operating Manual ● Genius
®
of the transmitter in watts (W) according to the manufacturer.
Maximum Length
RF emission, CISPR 1 - Class A / Group 1
Harmonic current emission: IEC61000-3-2
Voltage fluctuation: IEC61000-3-3
Immunity to electrostatic discharge: IEC61000-4-2
Immunity to electrical fast transient bursts: IEC61000-4-4
Less than 3 m
Immunity to surges: IEC61000-4-5
Immunity to voltage dips, brief interruptions, and voltage variation:
IEC61000-4-11
Conducted immunity - Radiofrequency conducted disturbance: IEC61000-4-6
Radiated immunity - Electromagnetic fields: IEC61000-4-3
Endodontic Motor ● J28629 ● V4 ● (16) ● 10/2016 ● NO69US010F
Complies with:
® endodontic motor. The text, graphics, and icons