"Kentila" Q switches Alexandria laser system - Taiwan Registration be2de80886408665d9e8c6fd32d4a73a
Access comprehensive regulatory information for "Kentila" Q switches Alexandria 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 be2de80886408665d9e8c6fd32d4a73a and manufactured by CANDELA CORPORATION. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..
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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
Apr 24, 2008
Apr 24, 2023