MagniFuse® Bone Graft - SFDA Registration ME0000000280SFDAA00040
Access comprehensive regulatory information for MagniFuse® Bone Graft in the Saudi Arabia medical device market through Pure Global AI's free database. This Class II device is registered with Saudi Arabia SFDA under registration number ME0000000280SFDAA00040 and manufactured by Medtronic Sofamor Danek USA, Inc..
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.
Resorbable Calcium Salt Bone Void Filler Device
MagniFuse® Bone Graft is comprised of human bone allograft tissue matrix in a resorbable mesh pouch to yield a high performance allograft product having a particular physical form and handling property. No additional carrier is added to the allograft material.
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