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“Caulk” SDR Plus - Taiwan Registration 7fdf89205dbc4f9fd1d48223012545da

Access comprehensive regulatory information for “Caulk” SDR Plus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7fdf89205dbc4f9fd1d48223012545da and manufactured by DENTSPLY CAULK. 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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7fdf89205dbc4f9fd1d48223012545da
Registration Details
Taiwan FDA Registration: 7fdf89205dbc4f9fd1d48223012545da
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Device Details

“Caulk” SDR Plus
TW: “寇克”思迪爾帕拉斯流動性樹脂補牙材
Risk Class 2
MD

Registration Details

7fdf89205dbc4f9fd1d48223012545da

Ministry of Health Medical Device Import No. 032836

DHA05603283608

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3690 Resin tusk wood

Imported from abroad

Dates and Status

Sep 08, 2019

Sep 08, 2024