Taiwan FDA registration eec8c4bdc7d6dbfdc0a348e893af3df3
"Medtronic" extended arterial cannula
TW: "美敦力" 延長型動脈套管
Taiwan·Risk Class 2·Medtronic Perfusion Systems;; Medtronic Inc.·Registered Apr 21, 2005 – Apr 21, 2030ActiveRegistration details
- Analysis ID
- eec8c4bdc7d6dbfdc0a348e893af3df3
- Customs Code
- DHA00601122508
Company information
- Manufacturer
- Medtronic Perfusion Systems;; Medtronic Inc.
- 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
- Import Information
- import
Dates and status
- Registration Date
- Apr 21, 2005
- Expiry Date
- Apr 21, 2030
About this record
Access comprehensive regulatory information for "Medtronic" extended arterial cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eec8c4bdc7d6dbfdc0a348e893af3df3 and manufactured by Medtronic Perfusion Systems;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices