Taiwan FDA registration 408d8167919676382b9fa7b950870a1f
"Croix Martin" unipolar argon electrode
TW: “凱樂思馬丁”單極氬氣電極
Taiwan·Risk Class 2·KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG·Registered Jul 27, 2021 – Jul 27, 2026ExpiredRegistration details
- Analysis ID
- 408d8167919676382b9fa7b950870a1f
- Customs Code
- DHA05603479201
Company information
- Manufacturer
- KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG
- Manufacturer Country
- Germany
- Authorized Representative
- KLS MARTIN 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
- Jul 27, 2021
- Expiry Date
- Jul 27, 2026
About this record
Access comprehensive regulatory information for "Croix Martin" unipolar argon electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 408d8167919676382b9fa7b950870a1f and manufactured by KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG. The authorized representative in Taiwan is KLS MARTIN TAIWAN LTD..
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