Taiwan FDA registration 61c171096a2bd393b266a3d2e278dba9
"Pinabo" microcatheter
TW: “彼娜波”微導管
Taiwan·Risk Class 2·PENUMBRA, INC.·Registered Mar 29, 2012 – Mar 29, 2017CancelledRegistration details
- Analysis ID
- 61c171096a2bd393b266a3d2e278dba9
- Customs Code
- DHA00602330904
Company information
- Manufacturer
- PENUMBRA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
Product details
- 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
Dates and status
- Registration Date
- Mar 29, 2012
- Expiry Date
- Mar 29, 2017
- Cancellation Date
- Nov 26, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Pinabo" microcatheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61c171096a2bd393b266a3d2e278dba9 and manufactured by PENUMBRA, INC.. The authorized representative in Taiwan is LORION ENTERPRISES INC..
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