GentleYAG Laser System
Candela Corporation
8501-00-1766 Revision F
CONFIDENTIAL
Page 25
Weight
210 lbs (95 kg)
Cryogen
HFC 134a
Voltage and Current
220-230V 50/60HZ single phase 16A
Miscellaneous (per EN60601-1):
Type of protection against electric
shock
Class I equipment
Degree of protection against
electric shock offered by the
applied part
Type “B”
Sterilization method
None required
Ingress protection
Ordinary enclosed
Not “AP” or “APG” equipment
The
GentleYAG
Laser System is a Class 4 laser product with a Class 1 aiming beam
per EN60825-1 Laser Hazard Classification. The
GentleYAG
Laser System is
a Class
II medical device per FDA 21 CFR 878.4810, and a Class llb (Rule 9), non-invasive,
active device according to Annex lX of Directive 93/42/EEC.
GentleYAG
comply with 21 CFR 1040.10 and
1040.11 except for deviations pursuant to Laser
Notice No. 50, dated July 26, 2001
Regulatory
Classifications
Table 1-1
Specifications
Cont.
Summary of Contents for GentleYAG
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