"Kendela" holographic super-picosecond laser system - Taiwan Registration f2610acca156dce14ce7e52860c33f87
Access comprehensive regulatory information for "Kendela" holographic super-picosecond laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f2610acca156dce14ce7e52860c33f87 and manufactured by NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation, 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
f2610acca156dce14ce7e52860c33f87
DHA05602987903
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
Jun 03, 2017
Jun 03, 2027