Intended Use - Memmert UN Série Mode D'emploi Rapide

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Intended use

Product
Intended use
UN
plus
This appliance is intended exclusively for
xx
UF
plus
heating up non-explosive substances and
xx
IN
plus
objects. Any other use is improper and
xx
IF
plus
may result in hazards and damage.
xx
UN
The appliance is not explosion-proof
xx
UF
(does not comply with the German occu-
xx
IN
pational health and safety regulation VBG
xx
IF
24). The appliance may only be loaded
xx
with materials and substances which can-
not release any toxic or explosive vapours
at the set temperature and which cannot
explode, burst or ignite.
The appliance may not be used for the
drying, evaporation and burning-in of
paints or similar materials, the solvents
of which could form an explosive mixture
when combined with air. If there is any
doubt as to the composition of materi-
als, they must not be loaded into the
appliance. Potentially explosive gas-air
mixtures must not form, neither in the
working chamber nor in the direct vicinity
of the appliance.
Product
Intended use as a medical device
UN
mplus
The appliance is used to heat fango, sili-
xx
UF
mplus
cate and APS packs for physical therapy
xx
UN
m
and to keep them warm.
xx
IN
m
xx
IN
mplus
The appliance may be used for tempera-
xx
ture control of rinsing and infusion solu-
IF
mplus
xx
tions and contrast agents.
10
Directives
Directive 2004/108/EC
amended (Directive of the Eu-
ropean Parliament and of the
Council on the approximation
of the laws of the Member
States relating to electromag-
netic compatibility). Standards
complied with:
DIN EN 61326:2004-05, EN
61326:1997, EN 61326/
A1:1998, EN 61326/A2:2001
EN 61326/A2:2003
Directive 2006/95/EC amend-
ed (Directive of the European
Parliament and of the Council
on the harmonisation of the
laws of Member States relat-
ing to electrical equipment
designed for use within cer-
tain voltage limits). Standards
complied with:
DIN EN 61 010-1 (VDE 0411
part 1)
DIN EN 61 010-2-010 (VDE
0411 part 2-010)
EN 61 010-1:2001, EN 61
010-2-010
Directive
Directive 93/42/EEC (Council
Directive concerning medical
devices)

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