“SDI” Capsule Mixer (Non-Sterile) - Taiwan Registration 577882efc181e9d6a5ce4b0a773f68ce
Access comprehensive regulatory information for “SDI” 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 577882efc181e9d6a5ce4b0a773f68ce and manufactured by SDI LIMITED. 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
577882efc181e9d6a5ce4b0a773f68ce
Ministry of Health Medical Device Import No. 022491
DHA09402249101
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

