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Bioinductive implant with Arthroscopic delivery system - SFDA Registration ME0000009018SFDAA00170

Access comprehensive regulatory information for Bioinductive implant with Arthroscopic delivery system 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 ME0000009018SFDAA00170 and manufactured by Smith & Nephew Inc..

This page provides complete registration details including product category (MD), 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
ME0000009018SFDAA00170
Bioinductive implant with Arthroscopic delivery system
SFDA Registration: ME0000009018SFDAA00170
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Product Information

bioabsorbable implant device that provides a layer of collagen over injured tendons.

Product Use

intended for the management and protection of tendon injuries.

Device Classification
Risk Class
Class III
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000009018SFDAA00170
Authorization ID
GHTF-2020-1615
Status
Active
Expire Date
August 15, 2023
Manufacturer
Manufacturer Name
Smith & Nephew Inc.
Model Information
Model ID(s)
72205306 72205307
Product Accessories

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