Taiwan FDA registration 79fbe17368e5504341a0f71ee3b5721b
"Abbott" Foss deep peripheral vascular balloon catheter
TW: “亞培”福斯深層周邊血管氣球導管
Taiwan·Risk Class 2·ABBOTT LABORATORIES VASCULAR ENTERPRISES LIMITED, DUBLIN, BERINGEN BRANCH·Registered Oct 29, 2007 – Oct 29, 2012CancelledRegistration details
- Analysis ID
- 79fbe17368e5504341a0f71ee3b5721b
- Customs Code
- DHA00601838003
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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Oct 29, 2007
- Expiry Date
- Oct 29, 2012
- Cancellation Date
- Mar 27, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Abbott" Foss deep peripheral vascular balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79fbe17368e5504341a0f71ee3b5721b 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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