Taiwan FDA registration ce69bd574c073e863a4f05d17452b591
"Delden" paste root canal filling material
TW: “黛爾登”糊劑根管充填材料
Taiwan·Risk Class 2·DiaDent Group International·Registered Oct 04, 2024 – Oct 04, 2029ActiveRegistration details
- Analysis ID
- ce69bd574c073e863a4f05d17452b591
- Customs Code
- DHA05603761606
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)
- F.3820 根管充填樹脂
- Import Information
- import
Dates and status
- Registration Date
- Oct 04, 2024
- Expiry Date
- Oct 04, 2029
About this record
Access comprehensive regulatory information for "Delden" paste 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 ce69bd574c073e863a4f05d17452b591 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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