LIGHTMED TruScan Pro – Operator’s Manual Rev. No. 01 Page 17 of 109
Indicates the optical radiation hazard of laser
products according to their degree as per IEC
60825-1:2007, 411/07.
Indicates the emergency laser stop button as
per IEC 60601-2-22-101.
Do not dispose with domestic household
waste. This equipment must not be disposed
of as unsorted municipal waste. Disposing of
WEEE together with normal waste may pose
a risk to the environment and to human health,
due to certain substances used in that
equipment as per EN 50419.
Type B applied part. One of the six ways of
applied part, which indicates that the medical
device does not need to touch the patient
when it is in use, or that it can be removed
immediately as per IEC 60417-2497.
For indoor use only. Indicates that this medical
device is an electrical equipment designed
primarily for indoor use as per IEC 60417-
5957.
Conformité Européene or European
Conformity. Indicates Manufacturer
declaration that the product complies with the
essential requirements of the relevant
European health, safety, and environmental
protection legislation as per 93/42/EEC,
Article 17.
Refer to instruction manual/booklet. Indicates
that the instruction manual/booklet must be
read prior to use as per ISO 7010-M002.
Class II equipment. Indicates that this
equipment meets the safety requirements
specified for Class II equipment as per IEC
60417-5172.
Electrical output information. Indicates that the
maximum output current is 5 amps and the
output voltage is 12 volts. Solid and dashed
lines signify DC output.
Indicates the remote interlock connector as
per IEC 60825-1-3-74 and IEC 60601-2-22-
112.
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