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Tendon Anchors (8) - SFDA Registration ME0000009018SFDAA00171

Access comprehensive regulatory information for Tendon Anchors (8) 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 ME0000009018SFDAA00171 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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SFDA Official Data
Class III
ME0000009018SFDAA00171
Tendon Anchors (8)
SFDA Registration: ME0000009018SFDAA00171
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Product Information

bioabsorbable implant devices that provide fixation of a prosthetic material to soft tissue.

Product Use

intended for fixation of prosthetic material to soft tissues.

Device Classification
Risk Class
Class III
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000009018SFDAA00171
Authorization ID
GHTF-2020-1615
Status
Active
Expire Date
August 15, 2023
Manufacturer
Manufacturer Name
Smith & Nephew Inc.
Model Information
Model ID(s)
72205201
Product Accessories

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