"Frieton" R&F system equipment (unsterilized) - Taiwan Registration 4a3dae94ced84660f6085932e406947a
Access comprehensive regulatory information for "Frieton" R&F system equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4a3dae94ced84660f6085932e406947a and manufactured by FRIADENT GMBH. The authorized representative in Taiwan is Taiwan Branch of American Denspie 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 scope of first-class identification of medical equipment management methods (intradental implant attachments [F.3980]).
F Dentistry
F.3980 Intradental implant manipulation equipment
import
Dates and Status
Apr 03, 2006
Apr 03, 2016
Apr 25, 2018
Cancellation Information
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