Taiwan FDA registration 070593cb51015ab8207c9341a0ac0b90
"Kellos Martin" bipolar electric knife
TW: “凱樂思馬丁”雙極電刀
Taiwan·Risk Class 2·KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG·Registered May 31, 2020 – May 31, 2030ActiveRegistration details
- Analysis ID
- 070593cb51015ab8207c9341a0ac0b90
- Customs Code
- DHA05603370409
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
- May 31, 2020
- Expiry Date
- May 31, 2030
About this record
Access comprehensive regulatory information for "Kellos Martin" bipolar electric knife in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 070593cb51015ab8207c9341a0ac0b90 and manufactured by KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG. The authorized representative in Taiwan is KLS MARTIN TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices