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“Cavex” Temporary Cement - Taiwan Registration dd653d4b9dcb109c8703c2d39efe1ed9

Access comprehensive regulatory information for “Cavex” Temporary Cement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd653d4b9dcb109c8703c2d39efe1ed9 and manufactured by CAVEX HOLLAND B.V.. The authorized representative in Taiwan is FOMED BIOTECH INC..

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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dd653d4b9dcb109c8703c2d39efe1ed9
Registration Details
Taiwan FDA Registration: dd653d4b9dcb109c8703c2d39efe1ed9
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Device Details

“Cavex” Temporary Cement
TW: “佳貝氏”臨時黏著劑
Risk Class 2
MD

Registration Details

dd653d4b9dcb109c8703c2d39efe1ed9

Ministry of Health Medical Device Import No. 036709

DHA05603670908

Company Information

Netherlands

Product Details

Details are as detailed as approved Chinese instructions

F Dentistry

F3275 Dental cement (Sminting)

Imported from abroad

Dates and Status

Aug 28, 2023

Aug 28, 2028