“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.
Device Details
Registration Details
80049c3e0640542191c7983b86afdfcb
Ministry of Health Medical Device Import No. 022492
DHA09402249203
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

