Saudi Arabia SFDA registration ME0000000280SFDAA00040
MagniFuse® Bone Graft
Saudi Arabia·Medical Device·Medtronic Sofamor Danek USA, Inc.·Class IIActiveProduct information
Resorbable Calcium Salt Bone Void Filler Device
Product use
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.
Device classification
- Risk Class
- Class II
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000280SFDAA00040
- Authorization ID
- MDMA-1-2019-0286
- Status
- Active
- Expire Date
- December 21, 2024
Manufacturer
- Manufacturer Name
- Medtronic Sofamor Danek USA, Inc.
Model information
- Model ID(s)
- 7509211INT, 7509212INT, 7509215INT, 7509221INT, 7509225INT, 7509141INT, 7509145INT, 7509007INT, 7509010INT, 7509014INT,
Product accessories
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About this record
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.
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