BIOTRONIK Selectra Catheters Manuel Technique page 9

Legend for the label
2
STERILIZE
NON
STERILE
CE mark
This product conforms with EC Directive 90/385/EEC relating to active
implantable medical devices. It is therefore designated with the CE mark. 
The product can be used in all European Union countries as well as in countries
that recognize the above-mentioned directive.
0123 (201
90/385/EEC
Manufacturing date of
the device
Use by
Storage temperature
BIOTRONIK order
number
Lot number
Sterilized with
ethylene oxide
Do not resterilize!
Single use only. 
Do not reuse!
Non-sterile
Consult the
instructions for use
Contents
Do not use if package
is damaged!
1)
8
European approval
mark
Inner diameter
Outer diameter
Total length
Working length
Dilator
Guiding catheter
(Selectra), various
curve shapes
(example)
Caution:
Federal (U.S.A.) law
restricts this product
to sale by, or on the
order of, a physician.
Protect from heat