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"Densberg Tianjin Factory" root tube paper needle (sterilization) - Taiwan Registration 912c6bbbe88a93f4c766816f34427bd3

Access comprehensive regulatory information for "Densberg Tianjin Factory" root tube paper needle (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 912c6bbbe88a93f4c766816f34427bd3 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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912c6bbbe88a93f4c766816f34427bd3
Registration Details
Taiwan FDA Registration: 912c6bbbe88a93f4c766816f34427bd3
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Device Details

"Densberg Tianjin Factory" root tube paper needle (sterilization)
TW: "็™ปๅฃซๆŸ ๅคฉๆดฅๅป " ๆ น็ฎก็ด™้‡(ๆป…่Œ)
Risk Class 1

Registration Details

912c6bbbe88a93f4c766816f34427bd3

DHA09600376304

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

QMS/QSD;; Chinese goods;; input

Dates and Status

Apr 23, 2019

Apr 23, 2029