"Kentila" Ress laser system - Taiwan Registration e8246a7c8f9a065f141ac66f6d3d4490
Access comprehensive regulatory information for "Kentila" Ress 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 e8246a7c8f9a065f141ac66f6d3d4490 and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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Device Details
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
import
Dates and Status
Sep 16, 2008
Sep 16, 2023