Taiwan FDA registration ef89c8695761e2bf29e0a7e7ff3d6d76
"Covidien" Horschtron electrosurgical instruments
TW: “柯惠”霍仕創摩電外科器械
Taiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Jan 20, 2020 – Jan 20, 2030ActiveRegistration details
- Analysis ID
- ef89c8695761e2bf29e0a7e7ff3d6d76
- Customs Code
- DHA05603317600
Company information
- Manufacturer
- COVIDIEN LLC;; 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
- import
Dates and status
- Registration Date
- Jan 20, 2020
- Expiry Date
- Jan 20, 2030
About this record
Access comprehensive regulatory information for "Covidien" Horschtron electrosurgical instruments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ef89c8695761e2bf29e0a7e7ff3d6d76 and manufactured by COVIDIEN LLC;; 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