Taiwan FDA registration 03e5999fff7df8e4a9feb0016a54a157
"Kellos Martin" electric burner
TW: “凱樂思馬丁”電燒鉗
Taiwan·Risk Class 2·KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG·Registered Dec 08, 2019 – Dec 08, 2029ActiveRegistration details
- Analysis ID
- 03e5999fff7df8e4a9feb0016a54a157
- Customs Code
- DHA05603301502
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
- Dec 08, 2019
- Expiry Date
- Dec 08, 2029
About this record
Access comprehensive regulatory information for "Kellos Martin" electric burner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03e5999fff7df8e4a9feb0016a54a157 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