Taiwan FDA registration bf591e1b4b45c365317b1ab51fa7e50a
"Medtronic" femoral arterial/venous cannula
TW: “美敦力”股動/靜脈套管
Taiwan·Risk Class 2·MEDTRONIC PERFUSION SYSTEMS·Registered Feb 16, 2011 – Feb 16, 2021CancelledRegistration details
- Analysis ID
- bf591e1b4b45c365317b1ab51fa7e50a
- Customs Code
- DHA00602205902
Company information
- Manufacturer
- MEDTRONIC PERFUSION SYSTEMS
- 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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
- Import Information
- import
Dates and status
- Registration Date
- Feb 16, 2011
- Expiry Date
- Feb 16, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Medtronic" femoral arterial/venous cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf591e1b4b45c365317b1ab51fa7e50a and manufactured by MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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