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“Denafit” Vacu-Mixer (Non-Sterile) - Taiwan Registration e34984b41864362cb101ce38c3e67eee

Access comprehensive regulatory information for “Denafit” Vacu-Mixer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e34984b41864362cb101ce38c3e67eee and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHINEO TECHNOLOGY CO., LTD..

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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e34984b41864362cb101ce38c3e67eee
Registration Details
Taiwan FDA Registration: e34984b41864362cb101ce38c3e67eee
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Device Details

“Denafit” Vacu-Mixer (Non-Sterile)
TW: “帝諾飛特” 維刻矽印模材自動混合機(未滅菌)
Risk Class 1
MD

Registration Details

e34984b41864362cb101ce38c3e67eee

Ministry of Health Medical Device Manufacturing No. 008917

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of dental and mercury instruments (F.3100) in the management of medical devices.

F Dental devices

F3100 Dental and mercury ware

Produced in Taiwan, China

Dates and Status

Mar 03, 2021

Mar 03, 2026