PENUMBRA SYSTEM 3 MAX REPERFUSION CATHETER - FDA Registration MDR-08923

Access comprehensive regulatory information for PENUMBRA SYSTEM 3 MAX REPERFUSION CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08923 and manufactured by Penumbra, Inc. in USA. The device was registered on November 21, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Asia Actual Consultancy, 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.