"Kentila" Jutemax laser system - Taiwan Registration 6d0bbfd2585cb5d9e4e4c57b0416b253
Access comprehensive regulatory information for "Kentila" Jutemax 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 6d0bbfd2585cb5d9e4e4c57b0416b253 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
6d0bbfd2585cb5d9e4e4c57b0416b253
DHA05602901803
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 08, 2016
Nov 08, 2026