Taiwan FDA registration 58f16fa8f3bc67c6c578824e762a149d
"Medtronic" double-foramen venous cannula
TW: "美敦力" 雙孔靜脈套管
Taiwan·Risk Class 2·Medtronic Perfusion Systems;; Medtronic Inc.·Registered Aug 15, 2002 – Aug 15, 2027ActiveRegistration details
- Analysis ID
- 58f16fa8f3bc67c6c578824e762a149d
- Customs Code
- DHA00601002801
Company information
- Manufacturer
- Medtronic Perfusion Systems;; Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Vacuum.
- 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
- Aug 15, 2002
- Expiry Date
- Aug 15, 2027
About this record
Access comprehensive regulatory information for "Medtronic" double-foramen 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 58f16fa8f3bc67c6c578824e762a149d and manufactured by Medtronic Perfusion Systems;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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