RED® 62 KIT Reperfusion Catheter + Penumbra Aspiration Tubing - FDA Registration CMDR-2023-01253A

Access comprehensive regulatory information for RED® 62 KIT Reperfusion Catheter + Penumbra Aspiration Tubing in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2023-01253A and manufactured by Penumbra, Inc. One Penumbra Place, Alameda, CA 94592 USA Mfd. By: Penumbra, Inc. - 630 Roseville Parkway, Roseville, CA 95747, USA in USA. The device was registered on January 12, 2023.

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.