"Pinabo" Pinabo system
Taiwan·Risk Class 2·PENUMBRA, INC.·Registered Aug 31, 2010 – Aug 31, 2020Cancelled- Analysis ID
- 7b3ee143097a1354e6115adfc4a31111
- Customs Code
- DHA00602134001
- Manufacturer
- PENUMBRA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
- Registration Date
- Aug 31, 2010
- Expiry Date
- Aug 31, 2020
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 7b3ee143097a1354e6115adfc4a31111 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.