Taiwan FDA registration 5dc6ff3746dd9acd496fe3a0c5c799e4

"DiaDent" Endodontic Root Canal Plugger (Non-Sterile)

TW: "戴德" 根管充填器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DIADENT GROUP INTERNATIONAL·Registered Sep 20, 2019 – Sep 20, 2024Expired
Registration details
Analysis ID
5dc6ff3746dd9acd496fe3a0c5c799e4
License Form
Ministry of Health Medical Device Import No. 020885
Customs Code
DHA09402088502
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
ASIANTOP ENTERPRISE CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F4565 Hand instruments for dental use
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 20, 2019
Expiry Date
Sep 20, 2024
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About this record

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.

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