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Cliniporator model EPS02 – User manual
9 TECHNICAL DATA
General Information
9.1
Manufacturer:
Commercial name:
Model:
Power Supply Specifications
9.2
Main switch voltage
Main switch frequency
Maximum power input
Protection fuses
Environmental Conditions
9.3
Working conditions
Room temperature
Relative humidity
Atmospheric pressure
Transport and Storage Conditions
Room temperature
Relative humidity
Atmospheric pressure
EN 60601-1 Classification
9.4
Protection against electrical risks
Applied part class
Liquids penetration
C L I N I P O R A T O R cannot be used in environments where there could be flammable anaesthetic
mixtures as specified by the EN 60601-1 standards. A mixture of the vapour of a flammable disinfection
or cleaning agent with air can be treated as a flammable anaesthetic mixture with air subject to national or
local regulations.
Medical Device Directive Classification 93/42/EEC and 2007/47/EEC
9.5
Class
Terms of Use
9.6
C L I N I P O R A T O R is suitable for continuous use. However, it is recommended to turn off the device
after every treatment session.
Technical Specifications
9.7
Dimensions (Width x Length x Height)
Weight
Output channels
Switching interval between each needle pair
Max. pulse energy (nominal)
IGEA S.p.A. Via Parmenide, 10/A 41012 Carpi (MO) Italy
CLINIPORATOR
EPS02
115/230 VAC
50-60 Hz
160 VA
2 type T 2.5A 250V - 5 x 20 mm Breaking Capacity: 35A L
from 10 to 40 °C
from 30% to 75%
from 700 hPa to 1060 hPa
from -20 to 50 °C
from 10% to 90%
from 500 to 1060 hPa
CLASS I
Defibrillation proof type BF applied parts.
IPX0 – No special protection on the device.
Al least IPX6 – Pedals.
.
IIa
46 x 65 x 156 cm
52 Kg
7
<60 ms
20 J with HV pulses
59
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