Taiwan FDA registration cdf23a42c7366462a5faa2910fcba845

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

TW: "美達"根管充填器(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·META BIOMED CO., LTD.·Registered May 24, 2017 – May 24, 2022Expired
Registration details
Analysis ID
cdf23a42c7366462a5faa2910fcba845
License Form
Ministry of Health Medical Device Import No. 017885
Customs Code
DHA09401788502
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
FRANKFURT TECHNOLOGY 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
May 24, 2017
Expiry Date
May 24, 2022
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About this record

Access comprehensive regulatory information for "META" 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 cdf23a42c7366462a5faa2910fcba845 and manufactured by META BIOMED CO., LTD.. The authorized representative in Taiwan is FRANKFURT TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including META BIOMED CO., LTD, 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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