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“Caulk” Aquasil Ultra Plus Impression Material - Taiwan Registration 2f0c9b05e7210fe4648c6810feee4ff3

Access comprehensive regulatory information for “Caulk” Aquasil Ultra Plus Impression Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f0c9b05e7210fe4648c6810feee4ff3 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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2f0c9b05e7210fe4648c6810feee4ff3
Registration Details
Taiwan FDA Registration: 2f0c9b05e7210fe4648c6810feee4ff3
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Device Details

“Caulk” Aquasil Ultra Plus Impression Material
TW: “寇克”新水精靈超印模材
Risk Class 2
MD

Registration Details

2f0c9b05e7210fe4648c6810feee4ff3

Ministry of Health Medical Device Import No. 032867

DHA05603286706

Company Information

United States

Product Details

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

F Dental devices

F3660 impression material

Imported from abroad

Dates and Status

Oct 14, 2019

Oct 14, 2024