Taiwan FDA registration 4be8cf039c41034d5c553482ff617e97
"Intec" Skobar peripheral vascular stent system
TW: “英泰克”斯可巴周邊血管支架系統
Taiwan·Risk Class 3·INVATEC S.P.A.·Registered Mar 24, 2010 – Mar 24, 2015CancelledRegistration details
- Analysis ID
- 4be8cf039c41034d5c553482ff617e97
- Customs Code
- DHA00602085707
Company information
- Manufacturer
- INVATEC S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- MEDTRONIC (TAIWAN) 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
- Mar 24, 2010
- Expiry Date
- Mar 24, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Intec" Skobar peripheral vascular stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4be8cf039c41034d5c553482ff617e97 and manufactured by INVATEC S.P.A.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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