Taiwan FDA registration 06f5df6e95b30aeefb491b3b8754cb4f
"Abbot" self-expanding perimeter bracket system
TW: “亞培”艾思博自擴型周邊支架系統
Taiwan·Risk Class 2·ABBOTT VASCULAR·Registered Jul 23, 2015 – Jul 23, 2020CancelledRegistration details
- Analysis ID
- 06f5df6e95b30aeefb491b3b8754cb4f
- Customs Code
- DHA05602746801
Company information
- Manufacturer
- ABBOTT VASCULAR
- Manufacturer Country
- United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and Urology;; E Cardiovascular Medical Sciences
- Product Type (Level 2)
- E.0001 Cardiovascular stents;; H.5010 Guides for gallant tubes and accessories
- Import Information
- import
Dates and status
- Registration Date
- Jul 23, 2015
- Expiry Date
- Jul 23, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Abbot" self-expanding perimeter bracket system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06f5df6e95b30aeefb491b3b8754cb4f and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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