"McLovever" Gidis root tube paper needle (unsterilized) - Taiwan Registration 9dd3f357a21f9832d5e1b03cc813d32b
Access comprehensive regulatory information for "McLovever" Gidis 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 9dd3f357a21f9832d5e1b03cc813d32b and manufactured by MAILLEFER INSTRUMENTS HOLDING. 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
import
Dates and Status
Apr 17, 2009
Apr 17, 2019
Jul 15, 2022
Cancellation Information
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