Asskea M20 Plus Instruction Manual page 62

The use of the recommended acces-
sories and spare parts (incl. trans-
formers and cables) in other devices
than the ASSKEA secretion aspira-
tors MPlus-series may increase the
emission of electromagnetic inter-
ference or reduce the electromagnetic
immunity. Damages caused by using
recommended accessories and spare
parts in other devices or by improper
use are not covered by warranty in
any case.
Only use the accessories and spare
parts with the ASSKEA secretion
aspirators MPlus-series!
Medical electrical equipment is sub-
ject to special precautionary measures
regarding electromagnetic compatibi-
lity and must be installed and opera-
ted in accordance with the EMC infor-
mation provided in the accompanying
documentation!
Portable and mobile RF communi-
cation equipment can affect medical
electrical equipment!
28
The ASSKEA secretion aspirators MPlus-
series meet the requirements of IEC
60601-1-2 / EN 60601-1-2 'Electromagnetic
Compatibility – Medical Electrical Equip-
ment'. Electromagnetic interference is there-
fore reduced to a minimum.
Guidance and Manufacturer's Declaration – Electromagnetic Emissions
The ASSKEA secretion aspirators MPlus-series are intended for operation in the electromagnetic
environment specified below. The customer or the user of an ASSKEA secretion aspirator MPlus-series
must ensure that it is operated in such an environment.
Emissions measurement
RF emissions CISPR 11
Harmonic emissions pursuant to
IEC 61000-3-2
Voltage fluctuations/ Flicker emis-
sions pursuant to IEC 61000-3-3
Compliance Electromagnetic Environment – Guidance
The ASSKEA secretion aspirators MPlus-se-
Class B
ries are appropriate for use in all facilities incl.
private residences and those directly connected
Class A
to the public power supply network that also
supplies buildings used for residential purpo-
Complies
ses.