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VenenWalker EMS AST-300S Mode D'emploi page 20

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20
Explanation of figures, symbols, warning statements and abbrevi-
ations on the equipment and in the operating instructions
Danger symbol: This symbol
indicates hazards. Read through
the associated safety instruc­
tions carefully and follow them.
Supplementary information
Read operating instructions
before use! This symbol appears
in blue on the device.
Protection class II
Polarity of the coaxial connector
(mains adapter)
Manufacturer
EU Representative
Medical device
Symbol for devices classified as
"Type BF" (level of protection
against electric shock)
IP21
Protected against solid foreign
objects 12.5 mm in diameter
and larger, and against vertically
falling drops of water.
Device serial number (Date
of production / consecutive
number)
Lot number
Date of manufacture
Importer
Indoor use only
03211_de-en-fr-nl_GM_A5_V4.indb 20
03211_de-en-fr-nl_GM_A5_V4.indb 20
Temperature limit: Indicates the
temperature limits to which the
medical device can be safely
exposed. The upper and lower
limits of temperature shall be
indicated adjacent to the upper
and lower horizontal lines.
Humidity limitation: Indicates the
range of humidity to which the
medical device can be safely
exposed. The humidity limitation
shall be indicated adjacent to the
upper and lower horizontal lines.
Atmospheric pressure limitation:
Indicates the range of atmos­
pheric pressure to which the
medical device can be safely
exposed. The atmospheric pres­
sure limitations shall be indicated
adjacent to the upper and lower
horizontal lines.
Devices bearing this symbol
were put into circulation after
13.08.2005 (DIN EN 50419). De­
vices labelled in this way meet
the labelling requirements of the
EU member states.
International recycling symbol
0413
With the CE mark, the manufacturer con­
firms that the product meets the require­
ments of the applicable EC directive and
complies with the "general requirements"
stipulated therein. The number 0413
alludes to the notified body (certifier).
Together these certify that the German
Medical Devices Act (MPG) has been
observed by the distributor.
19.04.2024 09:31:15
19.04.2024 09:31:15

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