Taiwan FDA registration c166a7dafe0743317ccc114ddfdf203f
Citus composite resin repair material
TW: 西萃思複合樹脂修復材
Registration details
- Analysis ID
- c166a7dafe0743317ccc114ddfdf203f
- Customs Code
- DHA05603673203
Company information
- Manufacturer Country
- United States
- Authorized Representative
- DHEF INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3690 Tree grease tooth material
- Import Information
- import
Dates and status
- Registration Date
- Sep 19, 2023
- Expiry Date
- Sep 19, 2028
About this record
Access comprehensive regulatory information for Citus composite resin repair material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c166a7dafe0743317ccc114ddfdf203f and manufactured by DENTAMERICA INC.;; PRIME DENTAL MANUFACTURING INC.. The authorized representative in Taiwan is DHEF INC..
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