Regulatory Information - PROTEOR DYNASTAR Instrucciones De Uso

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 Page 4 of 4