PROCART HANDLE - SFDA Registration ME0000000908SFDAA01895
Access comprehensive regulatory information for PROCART HANDLE in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ME0000000908SFDAA01895 and manufactured by Aesculap AG.
This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
surgical orthopaedic prosthesis
The OCT instrument set (OsteoChondral Transplantation) is used for the treatment of cartilage defects at the femoral condyles. The OCT instrument set is used to make osteochondral plugs and recipient drill holes.
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