Taiwan FDA registration 91f2118481d49185f7779da26f30dc8f
“Penumbra” Delivery Microcatheters
TW: “彼娜波”輸送微導管
Taiwan·Risk Class 2·MD·Penumbra, Inc.·Registered May 06, 2014 – May 06, 2024ExpiredRegistration details
- Analysis ID
- 91f2118481d49185f7779da26f30dc8f
- License Form
- Ministry of Health Medical Device Import No. 026140
- Customs Code
- DHA05602614001
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
- May 06, 2014
- Expiry Date
- May 06, 2024
About this record
Access comprehensive regulatory information for “Penumbra” Delivery Microcatheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 91f2118481d49185f7779da26f30dc8f and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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