Taiwan FDA registration 49d16a6ce6731e584fe3c96692c6097d

“DiaDent” DiaPaste Root Canal Filling Material

TW: “黛爾登”根管充填樹脂
Taiwan flagTaiwan·Risk Class 2·MD·DiaDent Group International·Registered Apr 16, 2021 – Apr 16, 2026Expired
Registration details
Analysis ID
49d16a6ce6731e584fe3c96692c6097d
License Form
Ministry of Health Medical Device Import No. 034430
Customs Code
DHA05603443003
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
SHI SEI INTERNATIONAL LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F3820 Root canal filling resin
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 16, 2021
Expiry Date
Apr 16, 2026
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About this record

Access comprehensive regulatory information for “DiaDent” DiaPaste Root Canal Filling Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49d16a6ce6731e584fe3c96692c6097d and manufactured by DiaDent Group International. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.

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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