Description Of The Symbols; Regulatory Information - PROTEOR 1D111 Instrucciones De Uso

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
st
CE marking and year of 1
Page 3 of 3
declaration