"Artini" transilluminator (unsterilized) - Taiwan Registration f36cc4f2db2d5eb02e3d04b212dc0781
Access comprehensive regulatory information for "Artini" transilluminator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f36cc4f2db2d5eb02e3d04b212dc0781 and manufactured by ARTINIS MEDICAL SYSTEMS B.V.. The authorized representative in Taiwan is MICROSTAR INSTRUMENTS 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 scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".
M Ophthalmology
M.1945 Transilluminator
import
Dates and Status
Mar 09, 2012
Mar 09, 2017
Apr 10, 2017
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ

