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“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.

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577882efc181e9d6a5ce4b0a773f68ce
Registration Details
Taiwan FDA Registration: 577882efc181e9d6a5ce4b0a773f68ce
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Device Details

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

Registration Details

577882efc181e9d6a5ce4b0a773f68ce

Ministry of Health Medical Device Import No. 022491

DHA09402249101

Company Information

Australia

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