Taiwan FDA registration eda9f8373b46360a5e8e4532ea2dd727
"Abbott" Ashber bracket system
TW: "亞培"亞士伯支架系統
Taiwan·Risk Class 2·ABBOTT LABORATORIES VASCULAR ENTERPRISES LIMITED, DUBLIN, BERINGEN BRANCH·Registered Oct 23, 2006 – Oct 23, 2011CancelledRegistration details
- Analysis ID
- eda9f8373b46360a5e8e4532ea2dd727
- Customs Code
- DHA00601736400
Company information
- Manufacturer Country
- Switzerland
- Authorized Representative
- WATTCAN INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5010 膽管用導管及其附件
- Import Information
- import
Dates and status
- Registration Date
- Oct 23, 2006
- Expiry Date
- Oct 23, 2011
- Cancellation Date
- Oct 25, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Abbott" Ashber 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 eda9f8373b46360a5e8e4532ea2dd727 and manufactured by ABBOTT LABORATORIES VASCULAR ENTERPRISES LIMITED, DUBLIN, BERINGEN BRANCH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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