Anspatch™ G1 Dissection Tools, Fluted Router - FDA Registration MDR-04916F

Access comprehensive regulatory information for Anspatch™ G1 Dissection Tools, Fluted Router in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04916F and manufactured by The Anspach Effort, Inc. 4500 Riverside Drive, Palm Beach Gardens, Florida, 33410, USA in USA. The device was registered on October 10, 2022.

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.