JRI VAIOS Mode D'emploi page 13

VAIOS® Shoulder System
IFU 155-032 (Issue 13)
March 2023
English
Do not resterilise
Medical Device
Authorised Representative in the
European Community
MRI Conditional
The device meets the essential
requirement of the European
Medical Device Regulations
Contains hazardous substances
Person Identification
(See Implant Card)
Health care centre or Doctor
(See Implant Card)
Date of Implantation
(See Implant Card)
Information website for patients
(See Patient Label)
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