Taiwan FDA registration 55779b56f6a09469e980cce3a28f7c1a
"Abbott" coronary artery envelope stent casting system
TW: "亞培"冠狀動脈包覆支架暨施放系統
Taiwan·Risk Class 3·ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH·Registered Dec 29, 2006 – Dec 29, 2016CancelledRegistration details
- Analysis ID
- 55779b56f6a09469e980cce3a28f7c1a
- Customs Code
- DHA00601764304
Company information
- Manufacturer
- ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH
- Manufacturer Country
- Germany
- 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.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- Dec 29, 2006
- Expiry Date
- Dec 29, 2016
- Cancellation Date
- Jun 26, 2018
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 envelope stent casting system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 55779b56f6a09469e980cce3a28f7c1a and manufactured by ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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