PROTEOR HYDEAL II Notice D'utilisation page 13

Relative humidity of the air: no restrictions
C. Disposal
The various components of this device are considered as special waste: elastomer, plastic, aluminium, titanium, steel, brass and oil.
They must be treated in accordance with current, applicable legislation.
D. Service life
It is advisable to arrange for a prosthetist/orthotist to check the product once a year.
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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