Taiwan FDA registration dae9fcd97704ee00097681eb7883517c
"Pinabo" Nuno intracranial delivery system
TW: “彼娜波” 紐諾顱內導入系統
Taiwan·Risk Class 2·Penumbra, Inc.·Registered Dec 11, 2023 – Dec 11, 2028ActiveRegistration details
- Analysis ID
- dae9fcd97704ee00097681eb7883517c
- Customs Code
- DHA05603677600
Company information
- Manufacturer
- Penumbra, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Dec 11, 2023
- Expiry Date
- Dec 11, 2028
About this record
Access comprehensive regulatory information for "Pinabo" Nuno intracranial delivery system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dae9fcd97704ee00097681eb7883517c and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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