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"DIADENT" Gutta Percha Points (Non-Sterile) - Taiwan Registration 836d2b9be3e3db400ae9fad25c752889

Access comprehensive regulatory information for "DIADENT" Gutta Percha Points (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 836d2b9be3e3db400ae9fad25c752889 and manufactured by DIADENT GROUP INTERNATIONAL (KOREA & INTERNATIONAL). The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.

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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836d2b9be3e3db400ae9fad25c752889
Registration Details
Taiwan FDA Registration: 836d2b9be3e3db400ae9fad25c752889
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Device Details

"DIADENT" Gutta Percha Points (Non-Sterile)
TW: "้ป›็ˆพ็™ป" ้ฆฌไพ†่† ้‡(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

836d2b9be3e3db400ae9fad25c752889

Ministry of Health Medical Device Import No. 015184

DHA09401518401

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".

F Dental devices

F3850 Male-Glue

Imported from abroad

Dates and Status

Apr 30, 2015

Apr 30, 2025