Taiwan FDA registration de1b309d62d99b86d6cdb8d940ad78cc
"Covidien" scouring tonsillectomy device
TW: “柯惠”百潔扁桃腺切除裝置
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered Nov 22, 2022 – Nov 22, 2027ActiveRegistration details
- Analysis ID
- de1b309d62d99b86d6cdb8d940ad78cc
- Customs Code
- DHA05603610107
Company information
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Nov 22, 2022
- Expiry Date
- Nov 22, 2027
About this record
Access comprehensive regulatory information for "Covidien" scouring tonsillectomy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de1b309d62d99b86d6cdb8d940ad78cc and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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