Protected against access to
dangerous parts with
fi
ngers.
Protected against solid foreign
bodies with a diameter of 12 mm
or larger.
Not
protected
against
ingress of
water.
Speci
fi
cations for use as a medical device
Name: Ultrasonic
homogeniser
UMDNS nomenclature (ECRI / DIMDI):
17-125
Purpose:
see chapter 1.2.
Medical device pursuant to
Directive 98/79/EC for in-vitro diagnostic medical devices:
Category 5 device (miscellaneous)
Type, model, serial number, year of manufacture:
See type plate on the generator for
information
The homogeniser has been inspected pursuant to norms currently in effect and must be installed
and put into operation pursuant to EMC directions; information in this regard is found in the
appendix.
Speci
fi
cations pursuant to the German Medical Devices Operator Ordinance (MPBetreibV):
Start-up on location, functional check
and personnel training (section 5):
not required
Technical safety check (STK) (section 6):
no speci
fi
cations
Technical measurement check (MTK) (section 11): not applicable
e-procurement
e-cl@ss:
HD device classi
fi
cation:
32-08-02-02
HD accessories classi
fi
cation: 32-08-92-03
1.4.2
Technical data, ultrasonic transducers (UW)
UW 2070 / UW 2200
PZT ultrasonic oscillating system:
Start/Stop key:
Suitable for continuous
operation:
Frequency:
20 kHz
Weight:
1.2 kg
Dimensions:
Ø 70 × 120 mm
Degree of protection:
IP 20 according to
DIN 60529
For environmental conditions, see chapter 1.4.1.
10 / 44
51436a GB/2017-10
1
electronic GmbH & Co. KG • Heinrichstraße 3-4 • 12207 Berlin • Deutschland • info@bandelin.com
