Taiwan FDA registration d9c295bc7b5e03a4263d64896ec9238a
“Friadent” ANKYLOS Balance Abutment System
TW: “飛雅登”安可平衡式植牙支柱系統
Taiwan·Risk Class 2·MD·DENTSPLY IMPLANTS MANUFACTURING GMBH·Registered Feb 04, 2013 – Feb 04, 2028ActiveRegistration details
- Analysis ID
- d9c295bc7b5e03a4263d64896ec9238a
- License Form
- Department of Health Medical Device Import No. 024657
- Customs Code
- DHA00602465706
Company information
- Manufacturer
- DENTSPLY IMPLANTS MANUFACTURING GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order. Increased efficiency: as detailed in Chinese copy of the single approval.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3630 Dental bridges for bone explants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 04, 2013
- Expiry Date
- Feb 04, 2028
About this record
Access comprehensive regulatory information for “Friadent” ANKYLOS Balance Abutment System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d9c295bc7b5e03a4263d64896ec9238a and manufactured by DENTSPLY IMPLANTS MANUFACTURING GMBH. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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