23
English
Ι
SPECIFICATIONS
Generator frequency
:
27.12 MHz, ± 0.6%
Output power
:
continuous HF max. 400 W */**
pulsed HF max. 1000 W (peak) */**
Pulse duration
:
ca. 400 µs
Pulse repetition frequency
:
15 - 200 Hz adjustable in 10 steps
Timer
:
0 - 30 min.; with acoustic signal and automatic switch-off
** Models for Canada and the USA have different specifications. Please consult your supplier.
*
Measured with 70 Ohm standard phantom (art.nr. 1462.471).
TECHNICAL DATA
Mains supply
:
220 - 240 V / 50 Hz (art.nr. 1419.942)
:
240 V / 50 Hz (art.nr. 1419.962)
:
115 V / 50 Hz (art.nr. 1419.982)
Mains voltage variation
:
max. ± 10%
Current consumption
:
max. 6 A (at 230 V)
Medical device classification
:
IIa (according to Medical Device Directive (93/42/EEC))
Leakage current
:
typically 350 µA (IEC requirement
≤
500 µA)
Safety class
:
Ι,
type BF according to IEC 60601-1
Dimensions
:
56 x 43 x 92.5 cm (w x d x h) without arms
Length electrode arms
:
93 cm
Weight
:
ca. 80 kg
Environment conditions for transport and storage
Environment temperature
:
-10° till +50° C
Relative humidity
:
10 till 95 %
Atmospheric pressure
:
500 till 1060 hPa
Environments conditions for normal use
Environment temperature
:
10° till 40° C
Relative humidity
:
10 till 90 %
Atmospheric pressure
:
500 till 1060 hPa
Classification
Medical class IIa
This equipment complies with all requirements of the Medical Device Directive (93/42/EEC).
International safety standard IEC 60601-1
Non-ionising radiation
Safety class I
The unit must be connected to a grounded wall socket.
Type BF (including Circuplodes)
The leakage current and the ground connection of the equipment meets the requirements of
IEC 60601-I and IEC 60601-2-3.
A copy of the test report will be sent on request.
Technical modifications reserved.
Содержание Curapuls 970
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