Specifications; Technical Data; Classification - Enraf Nonius Curapuls 670 Gebrauchsanweisung

13 Specifications

Frequency
Channels
Pulse duration
Pulse frequency
Pulse power
Mean power
Treatment time

14 Technical Data

Mains voltage
Mains frequency
Current consumption
Electrode cable
Medical device

classification

Safety class
Earth resistance
Earth leakage current
Earth leakage current
single fault condition
Dimensions
Weight (unit)
Electrode arm
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
14.1 Classification
EN
12
: 27.12 MHz (± 0.6 %)
: 2
: 65, 82, 110, 150, 200, 300, 400 µs (± 5%)
: 26, 35, 46, 62, 82, 110, 150, 200, 300, 400, 600 and 800 Hz (± 5%)
: 0 - 200 W (± 20%) into 50 ohm.
: 0 - 64 W (± 20%) into 50 ohm.
: 0 - 30 minutes (± 5%)
: 110-120 V, 220-240 V (± 10%)
: 50-60 Hz
: max. 1.6 A (at 230V)
: 50 ohm, 150 cm
: Ib (according to Medical Device Directive (93/42/EEC))
: I, type BF
: typically 0.12 ohm (IEC requirement ≤ 0.2 ohm.)
: typically 200 µA (IEC requirement ≤ 500 µA)
: typically 400 µA (IEC requirement ≤ 1000 µA)
: 39 x 40 x 93 cm (wxdxh)
: ca. 45 kg (excluding arm)
: ca. 2.5 kg
Medical class IIa
This equipment complies with all requirements of the Medical Device Directive
(93/42/EEG)
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 meet the
requirements of IEC 60601-1 and IEC 60601-2-3