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1556g GB/2019-02
1
electronic GmbH & Co. KG • Heinrichstraße 3-4 • 12207 Berlin • Deutschland • info@bandelin.com
/* In order to improve the effect the ultrasound is being modulated whereby a 4-fold ultrasonic nominal output value is yielded as
ultrasonic peak power.
Bath type
Order
No.
Interior dimensions
(L × W × D)
Operat-
ing
volume
Outlet
(valve)
Ultrasonic peak
power* / Ultra-
sonic nominal
output
Weight
(net)
Heating
power
Current
consump-
tion
(230 V)
Current
consump-
tion
(115 V)
mm
l
W / W
eff
kg
W
A
A
RK 512 H
795
300 × 240 × 200
8.7
G ½
860 / 215
8.3
400
2.7
5.4
RK 514
277
325 × 300 × 150
9.0
G ½
860 / 215
8.8
-
1.0
1.9
RK 514 H
207
325 × 300 × 150
9.0
G ½
860 / 215
8.8
600
3.6
7.1
RK 514 BH
263
325 × 300 × 200
12.5
G ½
860 / 215
9.8
600
3.6
7.1
RK 1028
322
500 × 300 × 200
19.0
G ½
1200 / 300
14.0
-
1.4
2.7
RK 1028 C
661
500 × 300 × 300
30.0
G ½
2000 / 500
24.5
-
2.2
-
RK 1028 H
324
500 × 300 × 200
19.0
G ½
1200 / 300
14.7
1300
7.0
14.0
RK 1028 CH
143
500 × 300 × 300
30.0
G ½
1200 / 300
23.4
1450
7.7
15.3
RK 1040
319
Ø 500 × 195
28.0
G ½
1520 / 380
19.4
-
1.7
3.4
RK 1050
323
600 × 500 × 200
41.0
G ½
2400 / 600
30.0
-
2.7
5.3
RK 1050 CH
184
600 × 500 × 300
60.0
G ½
2400 / 600
36.0
1950
11.1
17.9
Speci
fi
cations for use as a medical device
Name: Ultrasonic
bath
UMDNS nomenclature (ECRI / DIMDI):
14-263
Purpose:
See chapter 1.2.
Classi
fi
cation (Medical Device
Directive 93/42/EWG, Appendix IX):
Class I; active, non-invasive,
non-implantable medical device
Type, model, serial number, year of manufacture: See type plate on the rear side for information
The ultrasonic bath has been inspected pursuant to norms currently in effect and is to be installed
and put into operation pursuant to EMC directions.
Speci
fi
cations pursuant to the Medical Devices Operator Ordinance (MPBetreibV):
Startup on location, functional check
and personnel training (section 4):
not required
Technical safety controls, (STK, section 11):
no speci
fi
cations
Technical measurement controls, (MTK, section 14): not applicable
1.4.1 Electromagnetic ambient conditions (EMC)
The device was tested to DIN EN 61326-1 for electromagnetic compatibility (EMC) and complies
with the requirements for class B devices according to EN 55011.
It is suitable for use in facilities and areas which are directly connected to a public low-voltage
supply network, e.g. medical laboratory facilities.
It may generate radio interferences or disrupt the operation of devices nearby. It may be necessary
to take remedial measures such as realigning the device or a recon
fi
guring the ultrasonic bath or
the shield.
Summary of Contents for Sonorex Super RK 31
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