Taiwan FDA registration 20398633a0b283f93e0d27e6bf2481fb
"Kelis Martin" Matthew Maryland bipolar sealed instrument
TW: “凱樂思馬丁”馬修爾馬里蘭雙極密封器械
Taiwan·Risk Class 2·KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG·Registered Feb 09, 2021 – Feb 09, 2026ExpiredRegistration details
- Analysis ID
- 20398633a0b283f93e0d27e6bf2481fb
- Customs Code
- DHA05603428609
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
- For details, it is Chinese approved copy of the imitation order
- 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
- Feb 09, 2021
- Expiry Date
- Feb 09, 2026
About this record
Access comprehensive regulatory information for "Kelis Martin" Matthew Maryland bipolar sealed instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 20398633a0b283f93e0d27e6bf2481fb 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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