Taiwan FDA registration 23405cef262fb9958d06e4e17568cd18
"Abbott" coronary artery dilation stent system
TW: "亞培"冠狀動脈擴張支架系統
Taiwan·ABBOTT VASCULAR·Registered Nov 17, 1998 – Nov 17, 2013CancelledRegistration details
- Analysis ID
- 23405cef262fb9958d06e4e17568cd18
- Customs Code
- DHA00600892806
Company information
- Manufacturer
- ABBOTT VASCULAR
- Manufacturer Country
- United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Product Type (Level 1)
- 0399 Other artificial function substitutes
- Import Information
- import
Dates and status
- Registration Date
- Nov 17, 1998
- Expiry Date
- Nov 17, 2013
- Cancellation Date
- Sep 26, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Abbott" coronary artery dilation stent system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 23405cef262fb9958d06e4e17568cd18 and manufactured by ABBOTT VASCULAR. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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