"Laser Opp" Helios Q switched rubidium chromium laser - Taiwan Registration e0a31dec4dc32cc1e817e1192b78f3c8
Access comprehensive regulatory information for "Laser Opp" Helios Q switched rubidium chromium laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e0a31dec4dc32cc1e817e1192b78f3c8 and manufactured by LASEROPTEK Co., Ltd.. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..
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Device Details
Registration Details
e0a31dec4dc32cc1e817e1192b78f3c8
DHA05602871701
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.
Dates and Status
Aug 05, 2016
Aug 05, 2026