"Pinabo" Pinabo system
Taiwan·Risk Class 2·Penumbra, Inc.·Registered Jan 06, 2023 – Jan 06, 2028Active- Analysis ID
- 938dc7c6b1b776448d64da3f9a40942f
- Customs Code
- DHA05603626804
- Manufacturer
- Penumbra, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5600 Neurovascular mechanical clot removal device for the treatment of acute ischemic stroke
- Import Information
- import
- Registration Date
- Jan 06, 2023
- Expiry Date
- Jan 06, 2028
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Access comprehensive regulatory information for "Pinabo" Pinabo system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 938dc7c6b1b776448d64da3f9a40942f and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PENUMBRA, INC., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.