SEITE 13 - 148 x 210 mm - 44000118149/02 - SCHWARZ - 20-113 (kn)
13
ENGLISH
en
Warranty
3M Deutschland GmbH warrants this product will
be free from defects in material and manufacture.
3M Deutschland GmbH MAKES NO OTHER
WARRANTIES INCLUDING ANY IMPLIED
WARRANTY OF MERCHANTABILITY OR FITNESS
FOR A PARTICULAR PURPOSE. User is responsible
for determining the suitability of the product for
user’s application. If this product is defective within
the warranty period, your exclusive remedy and
3M Deutschland GmbH’s sole obligation shall be
repair or replacement of the 3M Deutschland GmbH
product.
Limitation of Liability
Except where prohibited by law, 3M Deutschland GmbH
will not be liable for any loss or damage arising from
this product, whether direct, indirect, special, incidental
or consequential, regardless of the theory asserted,
including warranty, contract, negligence, or strict liability.
Symbol Glossary
Reference Number
and Symbol Title
Symbol
Description of Symbol
ISO 15223-1
5.1.1
Manufacturer
Indicates the medical device
manufacturer as defined in EU
Directives 90/385/EEC,
93/42/EEC and 98/79/EC.
ISO 15223-1
5.1.3
Date of Manufacture
Indicates the date when the
medical device was manufac-
tured.
ISO 15223-1
5.1.5
Batch code
Indicates the manufacturer's
batch code so that the batch or
lot can be identified.
ISO 15223-1
5.1.6
Catalogue number
Indicates the manufacturer's
catalogue number so that the
medical device can be identi-
fied.
ISO 15223-1
5.1.7
Serial number
Indicates the manufacturer's
serial number so that a specific
medical device can be identi-
fied.
ISO 15223-1
5.3.7
Temperature limit
Indicates the temperature limits
to which the medical device can
be safely exposed.
ISO 15223-1
5.3.8
Humidity limitation
Indicates the range of humidity
to which the medical device can
be safely exposed.
ISO 15223-1
5.3.9
Atmospheric
pressure limitation
Indicates the range of atmo-
spheric pressure to which the
medical device can be safely
exposed.
ISO 15223-1
5.4.4
Caution
Indicates the need for the user to
consult the instructions for use
for important cautionary informa-
tion such as warnings and pre-
cautions that cannot, for a vari-
ety of reasons, be presented on
the medical device itself.
CE Mark
Indicates conformity to Euro-
pean Union Medical Device
Regulation or Directive.
Medical Device
Indicates the item is a medical
device.
Follow instructions
for use
To signify that the instructions
for use must be followed.
