Taiwan FDA registration 196589b3a6ffd4cc4536cf29bc8c4628
"Covidien" Iriss RF ablation accessories
TW: “柯惠”易瑞司射頻消融配件
Taiwan·Risk Class 2·Covidien llc;; Covidien·Registered Mar 31, 2023 – Mar 31, 2028ActiveRegistration details
- Analysis ID
- 196589b3a6ffd4cc4536cf29bc8c4628
- Customs Code
- DHA05603645901
Company information
- Manufacturer
- Covidien llc;; Covidien
- 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
- Mar 31, 2023
- Expiry Date
- Mar 31, 2028
About this record
Access comprehensive regulatory information for "Covidien" Iriss RF ablation accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 196589b3a6ffd4cc4536cf29bc8c4628 and manufactured by Covidien llc;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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