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BioComposite Interference Screw, Tapered Tip - SFDA Registration ME0000001945SFDAA00146

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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Class III
ME0000001945SFDAA00146
BioComposite Interference Screw, Tapered Tip
SFDA Registration: ME0000001945SFDAA00146
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Product 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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