"DORNIER" diode laser - Taiwan Registration 513d85d111c6e586f0e8f722f3aba3b2
Access comprehensive regulatory information for "DORNIER" diode laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 513d85d111c6e586f0e8f722f3aba3b2 and manufactured by Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Dornier MedTech America, Inc., 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
Registration Details
513d85d111c6e586f0e8f722f3aba3b2
DHA00601879404
Product Details
For details, it is Chinese approved copy of the imitation order
I General, Plastic Surgery and Dermatology
I.4810 Lasers for general surgical, orthopaedic and dermatological use
Contract manufacturing;; input
Dates and Status
Apr 15, 2008
Apr 15, 2028