
Technical data
40
Instructions for use Movita
Classification
EMC declaration
General information
The device was tested for electromagnetic
compatibility using accessories from the list of
accessories. Other accessories may only be used
if they do not compromise the electromagnetic
compatibility. The use of non-compliant
accessories may result in increased
electromagnetic emissions or decreased
electromagnetic immunity of the device.
The device may be used in the direct vicinity of
other devices only if Dräger has authorized this
device arrangement. If no authorization has been
given by Dräger, it must be ensured that the device
functions correctly in the desired arrangement
before using it. The instructions for use for the other
devices must be followed.
Electromagnetic environment
The emissions from this device were tested in the
following frequency ranges:
Protection class in accordance
with IEC 60601-1
Protection
class 1
Standards complied with
IEC 60601-1
IEC 60601-1-2
ISO 11197
Classification in accordance with
EU Directive 93/42/EEC
Annex IX
Class II b
UMDNS code
Universal Medical Device
Nomenclature System –
Nomenclature for medical
devices
18-046
Emissions
Compliance
Radiated emissions
Class A, group 1 (150 kHz to 30 MHz)
Conducted emissions
Class A, Group 1 (30 MHz to 1 GHz)