Taiwan FDA registration 0f021aba380e727e0e307ab51b0288c2
"Intec" Edmiró peripheral vascular balloon catheter
TW: “英泰克” 愛德米羅週邊血管氣球導管
Taiwan·Risk Class 2·Invatec S.p.A.·Registered May 05, 2009 – May 05, 2019CancelledRegistration details
- Analysis ID
- 0f021aba380e727e0e307ab51b0288c2
- Customs Code
- DHA00601983306
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.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- May 05, 2009
- Expiry Date
- May 05, 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" Edmiró 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 0f021aba380e727e0e307ab51b0288c2 and manufactured by Invatec S.p.A.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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