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“Renfert” Capsule Mixer (Non-Sterile) - Taiwan Registration 80049c3e0640542191c7983b86afdfcb

Access comprehensive regulatory information for “Renfert” Capsule 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 80049c3e0640542191c7983b86afdfcb and manufactured by RENFERT GMBH. 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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80049c3e0640542191c7983b86afdfcb
Registration Details
Taiwan FDA Registration: 80049c3e0640542191c7983b86afdfcb
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Device Details

“Renfert” Capsule Mixer (Non-Sterile)
TW: “倫芙” 牙科用膠囊混合器 (未滅菌)
Risk Class 1
MD

Registration Details

80049c3e0640542191c7983b86afdfcb

Ministry of Health Medical Device Import No. 022492

DHA09402249203

Company Information

Germany

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

Imported from abroad

Dates and Status

Apr 20, 2021

Apr 20, 2026