Taiwan FDA registration c686b420dee12dfa9bd306e57646b06c

"ANTHOGYR" ROOT CANAL POST (Non-Sterile)

TW: "安守吉" 根管柱釘 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ANTHOGYR SAS·Registered Apr 14, 2016 – Apr 14, 2026Expired
Registration details
Analysis ID
c686b420dee12dfa9bd306e57646b06c
License Form
Ministry of Health Medical Device Import No. 016397
Customs Code
DHA09401639700
Company information
Manufacturer
ANTHOGYR SAS
Manufacturer Country
France
Authorized Representative
WAVE PEP TRADE CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Center Column Nail (F.3810)".
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F3810 tube center column nail
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 14, 2016
Expiry Date
Apr 14, 2026
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About this record

Access comprehensive regulatory information for "ANTHOGYR" ROOT CANAL POST (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 c686b420dee12dfa9bd306e57646b06c and manufactured by ANTHOGYR SAS. The authorized representative in Taiwan is WAVE PEP TRADE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ANTHOGYR S.A., 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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