PENUMBRA COIL 400Ö COMPLEX SOFT - FDA Registration MDR-08298B

Access comprehensive regulatory information for PENUMBRA COIL 400Ö COMPLEX SOFT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08298B and manufactured by Penumbra, Inc. in USA. The device was registered on May 22, 2020.

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.