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Reco Pl. 3.5 - SFDA Registration ME0000000735SFDAA00661

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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SFDA Official Data
Class IIb
ME0000000735SFDAA00661
Reco Pl. 3.5
SFDA Registration: ME0000000735SFDAA00661
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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

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