Saudi Arabia SFDA registration ME0000000735SFDAA00661
Reco Pl. 3.5
Product information
Reconstruction plate for reconstructive pelvic and acetabular surgery
Product use
It is indicated for reconstructive pelvic and acetabular surgery
Device classification
- Risk Class
- Class IIb
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000000735SFDAA00661
- Authorization ID
- GHTF-2017-1106
- Status
- Active
- Expire Date
- December 06, 2023
Manufacturer
- Manufacturer Name
- Synthes GmbH
Product accessories
[]
About this record
Access comprehensive regulatory information for Reco Pl. 3.5 in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIb device is registered with Saudi Arabia SFDA under registration number ME0000000735SFDAA00661 and manufactured by Synthes GmbH.
This page provides complete registration details including product category (MD), manufacturer information, 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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