OPED VADOplex - VADOplex Technical Specifications; MDD Class and Certification; Rating and Power Supply Information; Environmental Conditions

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Useful details
Technical data
MDD class IIa (93/42/EEC, Annex IX, Rule 9)
Protection class I, Type B
CE certication No. CE 0123
Rating
Input: 230 V , 50/60 Hz, 0,4 A
Power supply: Manufactured by
M+R Multitronik GmbH
Power supply model: ACS60M-24
Fuses: T2AH250V
DIMDI No. 10-969 in accordance with UMDNS
Classication UMDNS
compression device intermittent
Code of the authority responsible DE CA 57 (Upper Bavaria)
Article-No. VXSY-07-1
This device is intended for continuous use. EMC tested in accordance with IEC 60601-1
and IEC 60601-1-2.
For information about potential electromagnetic interference and advice on how to avoid
or minimise such interference, please refer to the attachment of this user manual.
Environmental conditions for transport/storage
●
Temperature range: -25° C to 70° C
●
Relative humidity: up to 95 % without condensation
●
Ambient pressure: 700 hPa to 1.060 hPa
Environmental conditions during operation
●
Temperature range: 10° C to 40° C
●
Relative humidity: up to 95 % without condensation
●
Ambient pressure: 700 hPa to 1.060 hPa
Device dimensions
Height: 23 cm, overall
Depth without handle: 15.5 cm
Width: 35 cm
Weight: 4.0 kg
Warranty
The warranty complies with statutory regulations. The terms and conditions of business of OPED
GmbH also apply, where permissible.
0123
VADOplex
mmHg KPa mmHg KPa mmHg KPa
60 8,0 110 14,7 160 21,3
70 9,3 120 16,0 170 22,7
80 10,7 130 17,3 180 24,0
90 12,0 140 18,7 190 25,3
100 13,3 150 20,0 200 26,7
0123
10°C
40°C
Useful details
Conversion table
The device meets all essential requirements
of the applicable EU guidelines.
Before opening the device, unplug the
power supply.
Risk of explosion
Risk of falling
Type B applied part.
Observe accompanying documents!
Manufacturer
Date of manufacture
Temperature range
Data-Matrix
Safety Note
Single patient use only: The pads are to be
used for one patient only and may neither be
used for several patients nor refurbished.
The product and its packaging may not be
disposed of as household waste, but has to be
sent back to the manufacturer for disposal.
The manufacturer commits to the legally
compliant separation and collection of electrical
and electronic equipment based on the
requirements of ElektroG and the WEEE directive.