"Kellos Martin" bipolar electrofired instrument
Taiwan·Risk Class 2·KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG·Registered Sep 15, 2019 – Sep 15, 2029Active- Analysis ID
- 0e78fa8ca6f08dd2e4d2c6e5a39a118b
- Customs Code
- DHA05603284305
- Manufacturer
- KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG
- Manufacturer Country
- Germany
- Authorized Representative
- KLS MARTIN TAIWAN LTD.
- 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
- Registration Date
- Sep 15, 2019
- Expiry Date
- Sep 15, 2029
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Access comprehensive regulatory information for "Kellos Martin" bipolar electrofired instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0e78fa8ca6f08dd2e4d2c6e5a39a118b 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, 1 companies making similar products including KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG, and 1 recent registrations in the same category. 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.