24
Erbe recommends the processing procedures described in these
instructions for use. Equivalent different procedures are possible
if not explicitly excluded. It is incumbent on the user to ensure
the suitability of the actual procedures used by means of suit-
able measures (e.g. validation, routine monitoring, check of ma-
terial compatibility).
6
Disposal
Dispose of the product, packaging material and accessories (if
available) in accordance with the national guidelines and regu-
lation applicable in each case.
7
Symbols
ISO 15223-1 Medical devices – Symbols to be used with med-
ical device labels, labelling and information to be supplied
Ref. no. Symbol Title
Explanation
5.4.3
Consult in-
structions for
use
Indicates the need for the
user to consult the instruc-
tions for use.
5.1.6
Catalogue
number
Indicates the manufactur-
er’s catalogue number so
that the medical device can
be identified.
5.1.1
Manufacturer Indicates the medical device
manufacturer, as defined in
EU Directives 90/385/EEC,
93/42/EEC and 98/79/EC.
5.3.2
Keep away
from sunlight
Indicates a medical device
that needs protection from
light sources.
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