10. DESCRIPTION OF THE SYMBOLS
Manufacturer
11. REGULATORY INFORMATION
This product is a CE-marked medical device that is certified as conforming 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
INSTRUCTIONS FOR USE
Identified risk
CE marking and year of first declaration of
conformity
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