Taiwan FDA registration 79d772a8e768b0ec4510e7253a44b4d9
"Intec" Komis peripheral vascular stent system
TW: “英泰克”寇米斯週邊血管支架系統
Taiwan·Risk Class 2·INVATEC S.P.A.·Registered Jan 15, 2009 – Jan 15, 2019CancelledRegistration details
- Analysis ID
- 79d772a8e768b0ec4510e7253a44b4d9
- Customs Code
- DHA00601956303
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
- Jan 15, 2009
- Expiry Date
- Jan 15, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Intec" Komis peripheral vascular 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 79d772a8e768b0ec4510e7253a44b4d9 and manufactured by INVATEC S.P.A.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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