Labeling; Explanation Of Symbols - Chattanooga LightForce Serie Gebrauchsanleitung

Labeling

8.
8.1.

Explanation of Symbols

Symbol
Manufacturer
Date of manufacture
Catalog number
Serial number
Caution
Type B Applied Part
Do not dispose in unsorted
municipal waste (WEEE)
Laser Warning
Remote interlock connector
Foot Switch
Optical fiber applicator
Emergency Laser Stop
Fuse
Protective earth (ground)
Follow Instructions
Power On/Off
USB Port
IOIOI
VGA Port
Nemko-CCL Safety Mark with
NRTL indicators
60601-1
CE Marking of Conformity
Prescription devices
Authorized representative in the
European Community
RSR-000885-000 (6)
Title
Indicates the medical device manufacturer, as defined in EU Directives
90/386/EEC, 93/42/EEC and 98/79/EC.
Indicates the date when the medical device was manufactured.
Indicates the manufacturer's catalog, or model, number so that the medical device
can be identified.
Indicates the manufacturer's serial number so that a specific medical device can
be identified.
Indicates the need for the user to consult the instructions for use for important
cautionary information such as warnings and precautions that cannot, for a variety
of reasons, be presented on the medical device itself.
Refers to the part of the medical device which comes into physical contact with the
patient in order for the device to carry out its intended function.
Equipment must not be disposed of as unsorted municipal waste.
Warning label for class 2 and higher laser radiation
Identifies remote interlock connection port
Identifies connection port for foot switch
Identifies connection port for hand piece fiber
Button used to terminate laser emission and shutdown the device in the event of
an emergency.
To identify fuse boxes or their location.
Note: Not user replaceable.
To identify any terminal which is not intended for connection to an external
conductor for protection against electrical shock in case of a fault, or the terminal
of a protective earth (ground).
Note: This is located inside the device.
Indicates the need for the user to consult the instructions for use prior to
operating the device.
Push/push power button
Connection for software updates and Instant Replay Backup / Restore
For Manufacturer Use ONLY
Indicates compliance with the Certification Body (Nemko-CCL) requirements
regarding Electrical Safety (60601-1) in the US and Canada
Certification mark that indicates conformity with health, safety, and environmental
protection standards for products sold within the European Economic Area.
CAUTION – Federal law restricts this device to sale by or on the order of a licensed
practitioner licensed by the law of the State in which the practitioner practices to
use or order the use of the device
Indicates the Authorized representative (REP) in the European community (EC).
Description
Page 18 of 20