Service Life - PROTEOR 4 AXIS Instrucciones De Uso

D. Service life
It is advisable to arrange for an orthopaedic prosthetist to perform an annual check.
10. DESCRIPTION OF THE SYMBOLS
Manufacturer
11. REGULATORY INFORMATION
This product is a CE marked medical device, and certified compliant with Regulation (EU) 2017/745
12. NAME AND ADDRESS OF MANUFACTURER
PROTEOR SAS
6 rue de la Redoute – 21850 Saint-Apollinaire – France
Tel.: +33 3 80 78 42 42 – Fax: +33 3 80 78 42 15
cs@proteor.com – www.proteor.com
USER MANUAL
Risk identified CE marking and year of 1st declaration
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