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Follow instructions for use
Date of manufacture
Do not dispose of with domestic
waste
Data Matrix code
for product information
including UDI (Unique Device
Identification)
CE mark
with identification number
XXXX
of the Notified Body
The medical device with reference to electrical safety, mechanical safety
and fire prevention conforms to UL 60601-1:2006,
CAN/CSA-C22.2 No.601.1-M90:2005, CAN/CSA-C22.2 No. 60601-1:2008,
ANSI/AAMI ES 60601-1:2005 25UX (Control No.)
on the handpiece drive / handpiece sleeve
Non-sterilizable
Sterilizable
up to the stated temperature
Thermo washer disinfectable
Not suitable for intracardiac
application – Type BF appliance
Non-ionizing electromagnetic
radiation
Catalogue number
Serial number
DC – direct current
5
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