EasyManua.ls Logo

Penlon Prima 451 - Electromagnetic Compatibilty (EMC)

Penlon Prima 451
48 pages
Print Icon
To Next Page IconTo Next Page
To Next Page IconTo Next Page
To Previous Page IconTo Previous Page
To Previous Page IconTo Previous Page
Loading...
35 Prima 451 – User Manual
Appendix
Appendix 4. Electromagnetic compatibility (EMC)
Electromagnetc envronment
Ths devce s sutable for use n the specfed electromagnetc envronment The user should assure that t s used n an
electromagnetc envronment as descrbed below
hanges or modfcatons to ths devce, not expressly approved by Penlon Lmted, could result n EM ssues wth ths devce
ontact Penlon Lmted for more nformaton
The use of phones or RF emttng equpment near ths anaesthetc machne may cause nterference
Always montor anaesthetc machne operaton before and durng use on a patent
The essental performance of the Prma 451 anaesthetc machne s to provde controlled concentratons and flows of
anaesthesa gases nto a patent breathng system
WARNIN
The devce should not be used adacent to other manufacturer’s equpment If adacent use s necessary, the devce should
be observed to verfy normal operaton n the confguraton n whch t wll be used
ables, Transducers, and Accessores
WARNIN
The devce s EM-complant wth all cables, transducers and accessores suppled by Penlon Lmted
The use of cables, transducers and accessores other than those specfed may result n ncreased emssons or decreased
mmunty of ths devce
The use of cables, transducers and accessores suppled by Penlon Lmted on non-Penlon equpment may also result n
ncreased emssons or decreased mmunty of that equpment
Cables supplied by Penlon Limited
Category
Function Length (m)
A mans supply nput/output ports Hospital mains supply to the input port (cable is
fixed to the Prima 451.
≤3.9
A lnk Prma 451 equpped wth an AV-S MRI vent-
lator
Connects the Master on/off control on the
Prima 451 to the AV-S MRI ventilator
0.4
A200SP control cable (Prma 451 equpped wth an
AV-S MRI ventlator)
Connects (a) the spirometry sensors, and (b)
the absorber bag/vent switch on the A200SP
MRI absorber to the AV-S MRI ventilator
0.8
Oxygen sensor cable (Prma 451 equpped wth an
AV-S MRI ventlator)
Connects the oxygen sensor on the A200SP
MRI absorber to the AV-S MRI ventilator
2.7
Guidance and manufacturer’s declaration – electromagnetic emissions
Ths devce s ntended for use n the electromagnetc envronment specfed below The customer or user should assure that t
s used n such an envronment
Required test Compliance omments
RF emssons
ISPR 11
Group 1
Class A
lass A equpment s sutable for use n all locatons other than those
allocated n resdental envronments and those drectly connected
to a low voltage power supply network whch supples buldngs used
for domestc purposes, and may be used n domestc establshments
and those drectly connected to the publc low-voltage power supply
network that supples buldngs used for domestc purposes provded the
followng warnng s heeded
NOTE The EMISSIONS characterstcs of ths equpment make t
sutable for use n ndustral areas and hosptals (ISPR 11 class A) If
t s used n a resdental envronment (for whch ISPR 11 class B s
normally requred) ths equpment mght not offer adequate protecton
to rado-frequency communcaton servces The user mght need to take
mtgaton measures, such as relocatng or re-orentng the equpment
Harmonc emssons
IE 61000-3-2
Complies
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Complies

Related product manuals