"Kelis Martin" bipolar sealed instrument - Taiwan Registration fd3f7fc4e37eebdec6bce4f9f69673e2
Access comprehensive regulatory information for "Kelis Martin" 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 fd3f7fc4e37eebdec6bce4f9f69673e2 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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
I General, Plastic Surgery and Dermatology
I.4400 Cutting and hemostasis electric knives and accessories thereof
import
Dates and Status
Jul 03, 2018
Jul 03, 2028