Taiwan FDA registration 14dc7c4d0a1596a118656ebd975964e3

"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 Feb 12, 2015 – Feb 12, 2020Cancelled
Registration details
Analysis ID
14dc7c4d0a1596a118656ebd975964e3
License Form
Ministry of Health Medical Device Import No. 014924
Customs Code
DHA09401492400
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
ASIANTOP ENTERPRISE CO., LTD.
Product details
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
Feb 12, 2015
Expiry Date
Feb 12, 2020
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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 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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