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“Professional” Cavitron 300 Series Ultrasonic Scaler - Taiwan Registration e5d79ee68794538dca7ceb800694c883

Access comprehensive regulatory information for “Professional” Cavitron 300 Series Ultrasonic Scaler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5d79ee68794538dca7ceb800694c883 and manufactured by DENTSPLY PROFESSIONAL. 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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e5d79ee68794538dca7ceb800694c883
Registration Details
Taiwan FDA Registration: e5d79ee68794538dca7ceb800694c883
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Device Details

“Professional” Cavitron 300 Series Ultrasonic Scaler
TW: “普菲納”凱威壯三百系列超音波洗牙機
Risk Class 2
MD

Registration Details

e5d79ee68794538dca7ceb800694c883

Ministry of Health Medical Device Import No. 034687

DHA05603468701

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

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Dates and Status

Jun 25, 2021

Jun 25, 2026