Saudi Arabia SFDA registration ME0000001945SFDAA00146
BioComposite Interference Screw, Tapered Tip
Saudi Arabia·Medical Device·Arthrex, Inc·Class IIIActiveProduct information
Threaded or partially threaded and cannulated or non-cannulated screws used for graft fixation.
Product use
Interference Screws and RetroScrew are intended to be used for fixation of tissue including ligament or tendon to bone, or a bone/tendon to bone.
Tenodesis Screw: Intended to provide soft tissue reattachment (i.e. fixation of ligament and tendon graft tissue).
Device classification
- Risk Class
- Class III
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000001945SFDAA00146
- Authorization ID
- GHTF-2019-1275
- Status
- Active
- Expire Date
- January 13, 2020
Manufacturer
- Manufacturer Name
- Arthrex, Inc
Model information
- Model ID(s)
- AR-1360C
Product accessories
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About this record
Access comprehensive regulatory information for BioComposite Interference Screw, Tapered Tip in the Saudi Arabia medical device market through Pure Global AI's free database. This Class III device is registered with Saudi Arabia SFDA under registration number ME0000001945SFDAA00146 and manufactured by Arthrex, 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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