MODUS MEDARTIS CMF SYSTEM SET, 1.8 CORTICAL SCREWS, CROSS-DRIVE (EMERGENCY)
Philippines·Medartis AG·Switzerland·Issued November 22, 2019 – November 22, 2020- Product Name
- MODUS MEDARTIS CMF SYSTEM SET, 1.8 CORTICAL SCREWS, CROSS-DRIVE (EMERGENCY)
- Registration Number
- MDR-08949F
- Manufacturer
- Medartis AG
- Country of Origin
- Switzerland
- Importer/Distributor
- Dubbel Medical Corporation
- Issuance Date
- November 22, 2019
- Expiry Date
- November 22, 2020
Access comprehensive regulatory information for MODUS MEDARTIS CMF SYSTEM SET, 1.8 CORTICAL SCREWS, CROSS-DRIVE (EMERGENCY) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08949F and manufactured by Medartis AG in Switzerland. The device was registered on November 22, 2019.
This page provides complete registration details including manufacturer information, importer/distributor details (Dubbel Medical Corporation), 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.