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“DiaDent” DiaPaste Root Canal Filling Material - Taiwan Registration 49d16a6ce6731e584fe3c96692c6097d

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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49d16a6ce6731e584fe3c96692c6097d
Registration Details
Taiwan FDA Registration: 49d16a6ce6731e584fe3c96692c6097d
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Device Details

“DiaDent” DiaPaste Root Canal Filling Material
TW: “黛爾登”根管充填樹脂
Risk Class 2
MD

Registration Details

49d16a6ce6731e584fe3c96692c6097d

Ministry of Health Medical Device Import No. 034430

DHA05603443003

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3820 Root canal filling resin

Imported from abroad

Dates and Status

Apr 16, 2021

Apr 16, 2026

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