Taiwan FDA registration 860d02d6e38ae921363001b5deb1b67c
"Pinabo" Newno intracranial introduction system
TW: “彼娜波”紐諾顱內導入系統
Taiwan·Risk Class 2·Penumbra, Inc.·Registered Oct 23, 2009 – Oct 23, 2029ActiveRegistration details
- Analysis ID
- 860d02d6e38ae921363001b5deb1b67c
- Customs Code
- DHA00602025505
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 Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Oct 23, 2009
- Expiry Date
- Oct 23, 2029
About this record
Access comprehensive regulatory information for "Pinabo" Newno intracranial introduction system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 860d02d6e38ae921363001b5deb1b67c and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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