Saudi Arabia SFDA registration ME0000009018SFDAA00171
Tendon Anchors (8)
Saudi Arabia·MD·Smith & Nephew Inc.·Class IIIActiveProduct 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
[]
About this record
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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