CRYO-LINE
Manual for installation and use
OPTIKON 2000
Code 131002 EN
2014-02-06 Rev.F
5-2
5.3
TECHNICAL SPECIFICATIONS
PARAMETER
SPECIFICATIONS
Manufacturer:....................... OPTIKON 2000 S.p.A.
via del Casale di Settebagni, 13
00138 Rome - Italy
Model:................................ CRYO-LINE
Regulatory conformity: ............ 93/42/EEC Directive on medical devices
Technical standards: ............... EN 60601-1 ; EN 60601-1-1 ; EN 60601-1-2
ENVIRONMENTAL SPECIFICATIONS
Storage: .............................. temp. range between –10°C and +70°C, humidity 10-100%
(non-condensing)
Operating: ........................... temp. range b10°C and +40°C, humidity 30-75%.
ELECTRICAL SPECIFICATIONS
Input voltage: ....................... selectable at 100/120/220/240 Vac
Frequency: .......................... 50/60 Hz
Current consumption: ............. 80 VA
Fuses: ................................ 220-240 V: 1 A T
100-120 V: 2 A T
PNEUMATIC CIRCUIT
Supply gas………………………………… . medical N
2
0 or CO
2
in cylinder without siphon
Maximum input pressure .......... 70 bar - 1015 PSI
CLASSIFICATION OF THE INSTRUMENT ACCORDING TO IEC 60601-1
Type of protection against
electric shocks: ..................... Class I
Degree of protection against electric shocks:
Cryosurgical probe: ................ BF
Type of protection against
harmful entry of water: ........... IPX1
Degree of safety for use in the presence
of a flammable anaesthetic mixture
with air or oxygen
or nitrogen protoxide: ............. unsuitable
