"Dunshi Tianjin Factory" root tube paper needle (unsterilized) - Taiwan Registration ab47e445da137776ae64e9d9b957fa20
Access comprehensive regulatory information for "Dunshi Tianjin Factory" root tube paper needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ab47e445da137776ae64e9d9b957fa20 and manufactured by Dentsply Dental (TianJin) Co., Ltd.. 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 first level identification range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".
F Dentistry
F.3830 Root Canal
Input;; Chinese goods
Dates and Status
Dec 17, 2015
Dec 17, 2020
Jul 15, 2022
Cancellation Information
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