Taiwan FDA registration e1fc3f06637c1ccf4d706d01930190ea
"Pinabo" embolic ring system
TW: “彼娜波”栓塞環系統
Taiwan·Risk Class 2·PENUMBRA, INC.·Registered May 07, 2012 – May 07, 2022CancelledRegistration details
- Analysis ID
- e1fc3f06637c1ccf4d706d01930190ea
- Customs Code
- DHA00602356203
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)
- K Neuroscience
- Product Type (Level 2)
- K.5950 Artificial embolization device
- Import Information
- import
Dates and status
- Registration Date
- May 07, 2012
- Expiry Date
- May 07, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pinabo" embolic ring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1fc3f06637c1ccf4d706d01930190ea and manufactured by PENUMBRA, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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