DENTSPLY Cavitron Prophy-Jet Directions For Use Manual page 22

SECTION 14: Symbol Identification
AC POWER
TYPE B APPLIED PART EQUIPMENT
PROTECTIVE EARTH (GROUND)
Footswitch not for operating theatres
IPX1
Protection Class- IPX1
IPX1 Classification of ingress of water
Consult Instructions for Use
O/ I
AC Power Switch (0 = Off, | = On)
Footswitch
SECTION 15: Classifications
• Type of protection against electric shock:
• Degree of protection against electric shock:
• Degree of protection against the harmful ingress of water:
• Mode of operation:
• Degree of safety of application in the presence of a flammable
anaesthetic mixture with air or with oxygen or nitrous oxide:
• According to medical device directive:
SECTION 16: Disposal of Unit
U.S. - Dispose of the system components in accordance with state and local laws.
EU - Dispose of in accordance with the Waste Electrical and Electronic Equipment Directive 2002/96/EC of the European
Parliament and the Council of the European Union.
MEDICAL EQUIPMENT
WITH RESPECT TO ELECTRIC SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH
UL 60601-1CAN/CSA-C22.2 No. 601.1,
ANSI/AAMI ES60601-1 (2005, 3rd ed.)
CAN/CSA-C22.2 No. 60601-1 (2008),
13VA
This device complies with part 15 of the FCC Rules.
Operation is subject to the following two conditions:
1) this device may not cause harmful interference, and
2) this device must accept any interference received,
including interference that may cause undesired operation.
Foot pedal: FCC ID:TF3-DPD81861
IC: 4681B-DPD81861
Model: DPD81861
Base: FCC ID:TF3-DPD81842
IC: 4681B-DPD81842
Model: G138
Dispose of in accordance with the Waste Electrical and
Electronic Equipment Directive 2002/96/EC of the
WEEE
European Parliament and the Council of the European
Union
This is a wireless device.
This symbol is a mandatory marking for devices enter-
ing the European market to indicate conformity with
the essential health and safety requirements set out in
European Directives. The symbol may be accompanied
by a four-digit identification number of the notified
body.
Class 1
Type B
Ordinary
Continuous
Equipment not suitable for use in the presence of
flammable anaesthetic or oxygen.
IIA (rule 9)
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