Taiwan FDA registration bcc9e0ca543055913905c1cd471104e2
"Medtronic" Camboli biliary stent system
TW: “美敦力”康博立膽道支架系統
Taiwan·Risk Class 2·MEDTRONIC VASCULAR·Registered Aug 11, 2009 – Aug 11, 2014CancelledRegistration details
- Analysis ID
- bcc9e0ca543055913905c1cd471104e2
- Customs Code
- DHA00602010601
Company information
- Manufacturer
- MEDTRONIC VASCULAR
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) 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
- Aug 11, 2009
- Expiry Date
- Aug 11, 2014
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Medtronic" Camboli biliary stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bcc9e0ca543055913905c1cd471104e2 and manufactured by MEDTRONIC VASCULAR. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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