Taiwan FDA registration 2eeda9f22a4181d5c097a8ebff8ead83
"Covidien" 5mm endoscopic automatic vascular clamp
TW: “柯惠”5mm內視鏡自動血管夾
Taiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Sep 25, 2008 – Sep 25, 2028ActiveRegistration details
- Analysis ID
- 2eeda9f22a4181d5c097a8ebff8ead83
- Customs Code
- DHA00601923601
Company information
- Manufacturer
- COVIDIEN LLC;; Covidien
- Manufacturer Country
- Dominican Republic;;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
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Sep 25, 2008
- Expiry Date
- Sep 25, 2028
About this record
Access comprehensive regulatory information for "Covidien" 5mm endoscopic automatic vascular clamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2eeda9f22a4181d5c097a8ebff8ead83 and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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