Taiwan FDA registration 3d9b0d90a25b978e5d272a7db7b4bb33
“Penumbra” Benchmark Intracranial Access System
TW: “彼娜波”般馬可顱內通路系統
Taiwan·Risk Class 2·MD·Penumbra, Inc.·Registered Jul 24, 2018 – Jul 24, 2028ActiveRegistration details
- Analysis ID
- 3d9b0d90a25b978e5d272a7db7b4bb33
- License Form
- Ministry of Health Medical Device Import No. 031221
- Customs Code
- DHA05603122105
Company information
- Manufacturer
- Penumbra, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 24, 2018
- Expiry Date
- Jul 24, 2028
About this record
Access comprehensive regulatory information for “Penumbra” Benchmark Intracranial Access System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d9b0d90a25b978e5d272a7db7b4bb33 and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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