"Sharp Light" pulsed light system - Taiwan Registration f12e8d2b6a6bcc004f12af74983c9d96
Access comprehensive regulatory information for "Sharp Light" pulsed light system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f12e8d2b6a6bcc004f12af74983c9d96 and manufactured by SHARPLIGHT TECHNOLOGIES LTD.. The authorized representative in Taiwan is Dongzhe Riki Medical Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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
Mar 12, 2008
Mar 12, 2018
Feb 21, 2018
Cancellation Information
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