Taiwan FDA registration 14f8d9585e7846bdf558faf48f8c4ee4
“DiaDent” Dia-Root Bio Sealer
TW: “黛爾登”牙科根管封填材料
Registration details
- Analysis ID
- 14f8d9585e7846bdf558faf48f8c4ee4
- License Form
- Ministry of Health Medical Device Import No. 035089
- Customs Code
- DHA05603508902
Company information
- Manufacturer
- DiaDent Group International
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SHI SEI INTERNATIONAL LIMITED
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F3820 Root canal filling resin
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 12, 2021
- Expiry Date
- Dec 12, 2026
About this record
Access comprehensive regulatory information for “DiaDent” Dia-Root Bio Sealer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14f8d9585e7846bdf558faf48f8c4ee4 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. 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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