Attune™ Knee System Revision Tibial Vice - SFDA Registration ME0000000631SFDAA00342
Access comprehensive regulatory information for Attune™ Knee System Revision Tibial Vice 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 ME0000000631SFDAA00342 and manufactured by DePuy Ireland UC.
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 Instruments
The instruments used to implant orthopaedic prostheses do not have an indefinite function life. All reusable instruments are subjected to repeated stresses related to bone contact, impaction and routing, cleaning and sterilization process. It is essential that the surgeon and operating theatre staff are fully conversant with the appropriate surgical technique for the instruments and associated implant, if any.
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