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of the Elements Connect, including cables specified by the
Kerr Corporation.
• The EMISSIONS characteristics of this equipment make it
suitable for use in industrial areas and hospitals (CISPR 11
class A). If it is used in a residential environment (for which
CISPR 11 class B is normally required) this equipment
might not offer adequate protection to radio-frequency
communication services. The user might need to take
mitigation measures, such as relocating or re-orienting the
equipment.
PRECAUTIONS
• Do not use this device for any purpose other than its
intended use. The manufacturer is not responsible for any
injuries or damage caused by this.
• This device is not waterproof. Do not submerge the device in
water or let the device come into direct contact with water.
There is a risk of electric shock or device malfunction.
• Do not connect unsupported types of devices. The device
may break down or malfunction.
• When using or moving the device, do not throw or drop it.
The device may break down or malfunction.
• When using, be fully aware of the protective measures for
the patient and be prepared for possible risks.
• Check the patient's condition and device operation
during use.
• If the device is dropped during use, ensure that there is no
danger to the patient or user.
• When not using the device for a long period of time, store
it in a clean and dry place, where the temperature and
humidity do not change easily.
• If there are sign of smoke or burning, turn off the power
immediately, and take appropriate measures.
• If the device breaks down or has a problem, stop using it
immediately, and contact customer services.
• Any serious incident that has occurred in relation to the
device should be reported to the manufacturer and the
competent authority of the Member State.
• When selecting the proper file length for the procedure,
note that the total working length of the file is reduced by
2mm due to the deep set insert in the contra angle head and
might difficult the repositioning of the silicone stopper.
A longer file might have to be selected.
ADVERSE REACTIONS
None known.
SYMBOL DESCRIPTION
Full explanation of symbols used on Kerr packaging is located at:
http://www.kerrdental.com/symbols-glossary
Serial number
Authorized representative in the European Community
Original Equipment Manufacturer: Meta Systems Co., Ltd.
Private Label Manufacturer: Kerr Corporation
CE - Mark and identification number of notified body.
Product conforms to the essential requirements of the
Medical Device Directive 93/42/EEC
Type BF Applied Part
Humidity limitation
Fragile, handle with care
This way up
Sterilizable up to the stated temperature
Warning
WEEE Marking
Catalogue number
Medical Device
CAUTION: Federal law restricts this device to sale by or on
the order of a dentist
Date of manufacture
CSA Mark with "C/US" Indicator for Certified Products
Temperature limit
Atmospheric pressure limitation
Country of Manufacture
Keep dry
Refer to instruction manual
Caution
STEP-BY-STEP INSTRUCTIONS
PRECAUTION
The components and devices have not been disinfected or
sterilized prior to shipping. Please perform the necessary
cleaning and disinfection steps prior to patient treatment.
GETTING STARTED
Remove the device, contra angle, charging base, AC/DC adapter,
and power cord from their packaging.
1
Charging the Battery
• When using the device for the first time or after long-term
storage, charge the battery sufficiently before use.
• After connecting the power cord and AC/DC adapter, plug the
AC/DC adapter into the charging terminal on the back side of
the device and plug the power cord into the power supply.
• Insert the battery into the battery charging unit with the
charging terminal facing down. The charging indicator
illuminates orange indicating that the battery is being charged.
• While charging, the charging indicator lights up in orange.
• When charging is complete, the charging indicator lights
up blue.
4
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