Technical Specifications; Classification; Chapter 9 - Order Detail - Enraf Nonius Sonopuls 492 Instrucciones De Manejo

8.2. Technical specifications

Mains adapter
Type mains adapter
Mains voltage
Frequency
Output voltage
Max. Output current
Apparatus
Medical device classification
Safety class
Patient leakage current
Ditto, first fault condition
Safety tests
Dimensions
Weight
Environment conditions for transport and Storage
Environment temperature
Relative humidity
Atmospheric pressure
Environment conditions normal use
Environment temperature
Relative humidity
Atmospheric pressure

8.3. Classification

International safety norm
The Sonopuls 492 complies to the international norm for medical electrical devices IEC 60601-1, including
IEC 60601-2-5 (Ultrasound) and IEC 60601-2-10 (Electrical nerve stimulators).
I
Technical modifications reserved
For the ordering data of the Sonopuls 492, standard accessories and additional accessories refer to the
Catalogue for Physiotherapy and leaflet.
50
Medical class IIb
This equipment complies with all requirements of the Medical Device Directive (93/42/EEC).
The equipment has a safety earth (ground) connection, and must be connected to an earthed
(grounded) wall socket.
type BF, the equipment has a floating patient circuit.
: ENA-1550
: 100 - 240 Volt, +/- 10 %
: 50 / 60 Hz
: 15 Volt
: 3.3 Ampere
: IIb (according to Medical Device Directive (93/42/EEC)
: I, type BF, according to IEC 60601-1
: Better than IEC requirement (IEC < 100 µA)
: Better than IEC requirement (IEC < 500 µA)
: CE-MDD (TÜV Rheinland)
: 29 x 28 x 11 cm (w x d x h)
: 4 kg.
: -10° till +50° C
: 10 till 100 %
: 500 till 1060 hPa
: 10° till 40° C
: 10 till 90 % (non condensing)
: 500 till1060 hPa

CHAPTER 9 - ORDER DETAIL