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"Densberg" root tube paper needle (unsterilized) - Taiwan Registration 0fb434c38c73f3f7b254278243087645

Access comprehensive regulatory information for "Densberg" 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 0fb434c38c73f3f7b254278243087645 and manufactured by Dentsply Dental (TianJin) Co., Ltd.. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).

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.

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0fb434c38c73f3f7b254278243087645
Registration Details
Taiwan FDA Registration: 0fb434c38c73f3f7b254278243087645
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Device Details

"Densberg" root tube paper needle (unsterilized)
TW: "็™ปๅฃซๆŸ" ๆ น็ฎก็ด™้‡ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0fb434c38c73f3f7b254278243087645

DHA09600342408

Company Information

Product Details

It is limited to the first-level identification scope of the "Root Canal Paper Needle (F.3830)" of the Measures for the Classification and Grading of Medical Devices.

F Dentistry

F.3830 Root Canal

Input;; Chinese goods

Dates and Status

May 16, 2018

May 16, 2028