Taiwan FDA registration 51d2d5205d27e32a9a47af6bc490d661
"Covidien" endoscopic clamp
TW: “柯惠”內視鏡夾鉗
Taiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Mar 06, 2020 – Mar 06, 2025ExpiredRegistration details
- Analysis ID
- 51d2d5205d27e32a9a47af6bc490d661
- Customs Code
- DHA05603337809
Company information
- Manufacturer
- COVIDIEN LLC;; Covidien
- 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)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Mar 06, 2020
- Expiry Date
- Mar 06, 2025
About this record
Access comprehensive regulatory information for "Covidien" endoscopic clamp in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51d2d5205d27e32a9a47af6bc490d661 and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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