Taiwan FDA registration 6483afd87d90d8b3989ea5b297ec16d7
“Bard” FLAIR Endovascular Stent Graft
TW: “巴德”福萊爾周邊血管內套膜支架
Taiwan·Risk Class 3·MD·BARD PERIPHERAL VASCULAR, INC.·Registered Apr 21, 2015 – Apr 21, 2025ExpiredRegistration details
- Analysis ID
- 6483afd87d90d8b3989ea5b297ec16d7
- License Form
- Ministry of Health Medical Device Import No. 027268
- Customs Code
- DHA05602726803
Company information
- Manufacturer
- BARD PERIPHERAL VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 21, 2015
- Expiry Date
- Apr 21, 2025
About this record
Access comprehensive regulatory information for “Bard” FLAIR Endovascular Stent Graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6483afd87d90d8b3989ea5b297ec16d7 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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