"Kentila" Pro laser system - Taiwan Registration ea2ea4d23c8759f13b6dcd3144a1d2fa
Access comprehensive regulatory information for "Kentila" Pro 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 ea2ea4d23c8759f13b6dcd3144a1d2fa 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..
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Device Details
Registration Details
ea2ea4d23c8759f13b6dcd3144a1d2fa
DHA05602548300
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
Oct 02, 2013
Oct 02, 2028