Taiwan FDA registration d8cf11fa39d705b30f78373ddd8a9f80
"Intec" Reif High Pressure Peripheral Vascular Balloon Catheter
TW: “英泰克”瑞芙高壓週邊血管氣球導管
Taiwan·Risk Class 2·Invatec S.p.A.·Registered Jun 29, 2010 – Jun 29, 2020CancelledRegistration details
- Analysis ID
- d8cf11fa39d705b30f78373ddd8a9f80
- Customs Code
- DHA00602116802
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
- Jun 29, 2010
- Expiry Date
- Jun 29, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Intec" Reif High Pressure 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 d8cf11fa39d705b30f78373ddd8a9f80 and manufactured by Invatec S.p.A.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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