Philippines FDA registration MDR-08298C
PENUMBRA COIL 400™ COMPLEX STANDARD
Philippines·Penumbra, Inc.·USA·Issued April 15, 2020 – June 14, 2025Device information
- Product Name
- PENUMBRA COIL 400™ COMPLEX STANDARD
- Registration Number
- MDR-08298C
Manufacturer details
- Manufacturer
- Penumbra, Inc.
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Asia Actual Consultancy Inc.
Registration dates
- Issuance Date
- April 15, 2020
- Expiry Date
- June 14, 2025
About this record
Access comprehensive regulatory information for PENUMBRA COIL 400™ COMPLEX STANDARD in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08298C and manufactured by Penumbra, Inc. in USA. The device was registered on April 15, 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.
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