Taiwan FDA registration 0f41461e43c63088c7a1a24bdb0bfaa3
"Medtronic" single-hole venous cannula
TW: "美敦力" 單孔型靜脈套管
Taiwan·Risk Class 2·Medtronic Perfusion Systems;; Medtronic Inc.·Registered Aug 19, 2002 – Aug 19, 2027ActiveRegistration details
- Analysis ID
- 0f41461e43c63088c7a1a24bdb0bfaa3
- Customs Code
- DHA00601003501
Company information
- Manufacturer
- Medtronic Perfusion Systems;; Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- 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 19, 2002
- Expiry Date
- Aug 19, 2027
About this record
Access comprehensive regulatory information for "Medtronic" single-hole 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 0f41461e43c63088c7a1a24bdb0bfaa3 and manufactured by Medtronic Perfusion Systems;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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