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"Triodent" Rubber dam and accessories (Non-Sterile) - Taiwan Registration 90d777ff42350a5a8e1ee077612c22a2

Access comprehensive regulatory information for "Triodent" Rubber dam and accessories (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 90d777ff42350a5a8e1ee077612c22a2 and manufactured by TRIODENT LTD.. 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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90d777ff42350a5a8e1ee077612c22a2
Registration Details
Taiwan FDA Registration: 90d777ff42350a5a8e1ee077612c22a2
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Device Details

"Triodent" Rubber dam and accessories (Non-Sterile)
TW: "ๅ‰ตๆญ็™ป" ๆฉก็šฎ้šœๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

90d777ff42350a5a8e1ee077612c22a2

Ministry of Health Medical Device Import Registration No. 009012

DHA08400901203

Company Information

New Zealand

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Rubber Dam and Its Accessories (F.6300)".

F Dental devices

F6300 rubber dam and its accessories

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025