Spatz 3 Mode D'emploi page 44

For additional information, please contact your local distributor or:
Spatz FGIA Inc.
1801 S Perimeter Rd, Suite 130
Fort Lauderdale, FL 33309 USA
Tel: 1-516-303-0613
Fax: 1-516-303-0614
www.spatzmedical.com
MedNet EC-REP GmbH
Borkstrasse 10,
48163 Münster,
Germany
Device reference number
LOT Lot number in the format of
LLLLLL
Manufacturing date in the
format of YYYY-MM
2-year expiry date, based on
the manufacturing date, in the
format of YYYY-MM
Manufacturer
Medical Device
Health care center or doctor
Label Symbol Glossary
Authorized Representative in the
European Community
Attention, see instructions for use
Non-sterile
CE marking number of the
1023
notified body
Do not reuse
Unique Device Identifier
Implantation Date
only
Rx
1023
Only
LATEX FREE
Device does not contain natural
latex rubber
The device is restricted to sale by
or on the order of a physician
sterilized using ethylene oxide
Limits of temperature
Consult instruction of use
Don't use if package is damaged
Patient identification
Patient information website