"Laide" Westeron optical fiber dental light source and accessories (unsterilized) - Taiwan Registration 9df877fb9602117c50fadceed9bd7442
Access comprehensive regulatory information for "Laide" Westeron optical fiber dental light source and accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9df877fb9602117c50fadceed9bd7442 and manufactured by LED DENTAL INC.. The authorized representative in Taiwan is Yuanhong Instrument 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
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Light Source for Optical Fiber Dentistry (F.4620)".
F Dentistry
F.4620 Light source for optical fiber dentistry
import
Dates and Status
Feb 22, 2008
Feb 22, 2018
May 09, 2016
Cancellation Information
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