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Les langues disponibles
Treatment unit
Frequencies
Ultrasound mode
Intensity
Display
Indication accuracy
Timer
Contact control threshold
Treatment heads
1 MHz, large (standard)
1 MHz, small (optional)
3 MHz, large (optional)
3 MHz, small (optional)
*
SATP= Spatial Average Temporal Peak (mean pulse power).
** ERA = Effective Radiating Area, i.e. the effective area from which the ultrasound beam is emitted.
***BNR = Beam Nonuniformity Ratio, i.e. the ratio between the peaks and the average value of the intensity in the
ultrasound beam. A low BNR excludes the possibility of undesirably high energy concentrations in the
beam.
ERA and BNR are measured according to the FDA methods. All treatment heads are provided with contact control.
Mains voltage
Current consumption
Mains fuses
Patient leakage current
Ditto, first fault condition
Earth (ground) leakage current
Ditto, single fault condition
Earth resistance
Medical device classification
Safety class
Weight and dimensions
Safety tests
Environment conditions for transport and storage
Environment temperature
Relative humidity
Atmospheric pressure
Environments conditions for normal use
Environment temperature
Relative humidity
Atmospheric pressure
Medical class IIb
This equipment complies with all requirements of the Medical Device Directive
(93/42/EEC)
International Safety class IEC60601-1
* I
: The equipment has a safety earth (ground) connection, and must be
connected to an earthed (grounded) wall socket.
** BF : The equipment has a floating patient circuit. The Sonopuls 590 meets the
requirements of IEC 60601-1 and IEC 60601-2-5.
Copies of the test reports are available on request. Technical modifications reserved.
For the ordering data of the Sonopuls, standard accessories and additional accessories we refer to the Catalogue
for Physiotherapy.
:
1 MHz (± 0.2 %) and
:
continuous
pulsed at 100Hz, 2 ms pulse duration, duty cycle 20 %
pulsed at 48Hz, 4 ms pulse duration, duty cycle 20 %
pulsed at 16Hz, 12 ms pulse duration, duty cycle 20 %
:
0 - 2 W/cm
2
continuous and 0 - 3 W/cm
:
intensity in W/cm
2
or power in W (SATP*)
:
± 20 % (for any level above 10 % of maximum)
:
0 - 30 minutes, coupled to contact control
:
80 %
:
geometrical area 6.2 cm
parasitic side radiation max. 10 mW/cm
:
geometrical area 1.4 cm
parasitic side radiation max. 10 mW/cm
:
geometrical area 6.2 cm
parasitic side radiation zero
:
geometrical area 0.7 cm
parasitic side radiation zero
:
115 V~ 50/60 Hz ± 15% and 220-240 V~ 50/60 Hz ± 10%
:
max. 0.70 A at 115 V / 0.35 A at 230 V
:
2 x T1.6H250V
:
typically 10 µA (IEC requirement £ 100 µA)
:
typically 30 µA (IEC requirement £ 500 µA)
:
typically 60 µA (IEC requirement £ 500 µA)
:
typically 120 µA (IEC requirement £ 1000 µA)
:
typically 0.12 Ohm (IEC requirement £ 0.2 Ohm)
:
IIb (according to Medical Device Directive (93/42/EEC))
:
I* type BF**, according IEC 60601-1
:
6.1 kg / 36 x 33.5 x 12 cm
:
TÜV Rheinland
:
-10° till +50° C
:
10 till 95 %
:
500 till 1060 hPa
:
10° till 40° C
:
10 till 90 %
:
500 till 1060 hPa
3 MHz (± 0.2 %)
2
pulsed
2
, ERA** 5.0 cm
2
, BNR*** max. 6 type collimating,
2
2
, ERA 0.8 cm
2
, BNR max. 6 type diverging,
2
2
, ERA 5.0 cm
2
, BNR max. 6 type collimating,
2
, ERA 0.5 cm
2
, BNR max. 6 type diverging,
SPECIFICATIONS
TECHNICAL DATA
Type BF
ORDERING DATA
15
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