Taiwan FDA registration a48a58bfc129c63d3def42fde41b7540
"Abbott" Asbert bracket system
TW: “亞培”亞斯伯特支架系統
Taiwan·Risk Class 3·ABBOTT LABORATORIES VASCULAR ENTERPRISES LIMITED, DUBLIN, BERINGEN BRANCH·Registered Nov 16, 2009 – Nov 16, 2019CancelledRegistration details
- Analysis ID
- a48a58bfc129c63d3def42fde41b7540
- Customs Code
- DHA00602032500
Company information
- Manufacturer Country
- Switzerland
- 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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- Nov 16, 2009
- Expiry Date
- Nov 16, 2019
- 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 "Abbott" Asbert bracket system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a48a58bfc129c63d3def42fde41b7540 and manufactured by ABBOTT LABORATORIES VASCULAR ENTERPRISES LIMITED, DUBLIN, BERINGEN BRANCH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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