6
6
Safety Aspects
2. Safety Aspects
Th
he
e D900-P
P, D92
20-P
P, D93
30-P
P, FD2
2-P
P, SD2
2-P
P, MD2
2-P
P, FD1-P
P, FD3
3-P
P, RD2
2 Do
opplle
ers a
and
d th
he
eiir
pro
ob
be
es a
are
e d
de
esiigne
ed
d to
o h
hiigh
h sta
and
da
ard
ds o
of pe
erfo
orma
anc
ce
e, re
elliia
ab
biilliity a
and
d sa
afe
ety.
Ch
he
ec
ckks sh
ho
oulld
d a
allwa
ays b
be
e ma
ad
de
e a
afte
er c
ca
arryiing o
out a
any re
epa
aiirs o
or d
diisma
antlliing o
of th
he
e e
eq
quiipme
ent.
2.1 Safety
Regular inspections must be made to check the integrity of the unit, and to ensure that the
cable is not showing any signs of wear or is noisy when flexed.
For functional testing of specific product features, refer to the user manual.
If you require any assistance with safety testing your Dopplex equipment, contact Huntleigh
Healthcare Ltd or your supplier directly.
For the U.K. refer to the Health Equipment Information Document No 95 - Code Of Practice For
Acceptance Testing Of Medical Equipment.
The following safety summary should be read before operating or carrying out any of the
procedures described in this manual.
2.2 Maintenance
2.3 Cautions
Do not use the D900-P, D920-P D930-P, FD2-P, SD2-P, MD2-P, FD1-P, FD3-P, RD2 units in the
presence of flammable gases such as anaesthetic agents.
This product is not designed for sterile use. Do not use in the sterile field unless additional
barrier precautions are taken.
Do not
-
immerse in any liquid (except probe on D920-P, D930-P, FD1-P, FD3-P).
-
use solvent cleaners.
-
use high temperature sterilising processes (such as autoclaving).
-
use E-beam or gamma radiation sterilisation.