Taiwan FDA registration 51836f572f67fefd7a50ee09cb56e6ab
"Medtronic" provides flexible venous frequency ablation catheters
TW: ”美敦力”可柔速靜脈內射頻消融導管
Taiwan·Risk Class 2·Medtronic Inc.; Covidien·Registered Dec 17, 2007 – Dec 17, 2027ActiveRegistration details
- Analysis ID
- 51836f572f67fefd7a50ee09cb56e6ab
- Customs Code
- DHA00601850204
Company information
- Manufacturer
- Medtronic Inc.; Covidien
- Manufacturer Country
- Mexico;;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)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4400 Cutting and hemostasis electric knives and accessories thereof
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Dec 17, 2007
- Expiry Date
- Dec 17, 2027
About this record
Access comprehensive regulatory information for "Medtronic" provides flexible venous frequency ablation catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51836f572f67fefd7a50ee09cb56e6ab and manufactured by Medtronic Inc.; Covidien. 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