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"DiaDent" Endodontic Root Canal Plugger (Non-Sterile) - Taiwan Registration 14dc7c4d0a1596a118656ebd975964e3

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 14dc7c4d0a1596a118656ebd975964e3 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.

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14dc7c4d0a1596a118656ebd975964e3
Registration Details
Taiwan FDA Registration: 14dc7c4d0a1596a118656ebd975964e3
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Device Details

"DiaDent" Endodontic Root Canal Plugger (Non-Sterile)
TW: "ๆˆดๅพท"ๆ น็ฎกๅ……ๅกซๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

14dc7c4d0a1596a118656ebd975964e3

Ministry of Health Medical Device Import No. 014924

DHA09401492400

Company Information

Korea, Republic of

Product Details

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

Feb 12, 2015

Feb 12, 2020

Jul 15, 2022

Cancellation Information

Logged out

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