TRO-VENOCATH PLUS (FEP) I.V. Cannula (with Wings, with Injection Port Teflon (FEP)) - FDA Registration MDR-02282

Access comprehensive regulatory information for TRO-VENOCATH PLUS (FEP) I.V. Cannula (with Wings, with Injection Port Teflon (FEP)) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-02282 and manufactured by Troge Medical GmbH Hamburg, Germany in Germany. The device was registered on February 14, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Healthsolutions Enterprises 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.