"DiaDent" Endodontic Root Canal Plugger (Non-Sterile) - Taiwan Registration 5dc6ff3746dd9acd496fe3a0c5c799e4
Access comprehensive regulatory information for "DiaDent" Endodontic Root Canal Plugger (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 5dc6ff3746dd9acd496fe3a0c5c799e4 and manufactured by DIADENT GROUP INTERNATIONAL. The authorized representative in Taiwan is ASIANTOP ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DiaDent Group International, and 1 recent registrations in the same category. 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
5dc6ff3746dd9acd496fe3a0c5c799e4
Ministry of Health Medical Device Import No. 020885
DHA09402088502
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
F Dental devices
F4565 Hand instruments for dental use
Imported from abroad
Dates and Status
Sep 20, 2019
Sep 20, 2024

