EXPERT ANTEGRADE FEMORAL NAIL, LEFT - FDA Registration MDR-08383B
Access comprehensive regulatory information for EXPERT ANTEGRADE FEMORAL NAIL, LEFT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08383B and manufactured by Synthes GmbH in Switzerland. The device was registered on July 12, 2019.
This page provides complete registration details including manufacturer information, importer/distributor details (Johnson & Johnson (Phils), Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.
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Switzerland
MDR-08383B
EXPERT ANTEGRADE FEMORAL NAIL, LEFT
Registered medical device in Philippines
Device Information
Product Name
EXPERT ANTEGRADE FEMORAL NAIL, LEFT
Registration Number
MDR-08383B
Manufacturer Details
Manufacturer
Synthes GmbHCountry of Origin
Switzerland
Importer & Distribution
Importer/Distributor
Johnson & Johnson (Phils), Inc.Registration Dates
Issuance Date
July 12, 2019
Expiry Date
July 12, 2020

