Philippines FDA registration MDR-08923
PENUMBRA SYSTEM 3 MAX REPERFUSION CATHETER
Philippines·Penumbra, Inc.·USA·Issued November 21, 2019 – November 21, 2020Device information
- Product Name
- PENUMBRA SYSTEM 3 MAX REPERFUSION CATHETER
- Registration Number
- MDR-08923
Manufacturer details
- Manufacturer
- Penumbra, Inc.
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Asia Actual Consultancy, Inc.
Registration dates
- Issuance Date
- November 21, 2019
- Expiry Date
- November 21, 2020
About this record
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.
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