"Kendela" aurora pulsed light and laser system - Taiwan Registration acc8f22609ca7ac67abb2d54433fc99b
Access comprehensive regulatory information for "Kendela" aurora pulsed light and 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 acc8f22609ca7ac67abb2d54433fc99b 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
acc8f22609ca7ac67abb2d54433fc99b
DHA05602908709
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
Input;; The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". Contract manufacturing
Dates and Status
Nov 28, 2016
Nov 28, 2026