Taiwan FDA registration ccbf883c678dad1ce93e24a0da0c6638
"Sepudent" Baiyouding dentin restorative material
TW: “賽普敦特”百優定牙本質修補材
Taiwan·Risk Class 2·SEPTODONT·Registered Jan 21, 2013 – Jan 21, 2028ActiveRegistration details
- Analysis ID
- ccbf883c678dad1ce93e24a0da0c6638
- Customs Code
- DHA00602445507
Company information
- Manufacturer
- SEPTODONT
- Manufacturer Country
- France
- Authorized Representative
- EN-JYE INTERNATIONAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3820 根管充填樹脂
- Import Information
- import
Dates and status
- Registration Date
- Jan 21, 2013
- Expiry Date
- Jan 21, 2028
About this record
Access comprehensive regulatory information for "Sepudent" Baiyouding dentin restorative material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ccbf883c678dad1ce93e24a0da0c6638 and manufactured by SEPTODONT. The authorized representative in Taiwan is EN-JYE INTERNATIONAL CO., LTD..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices