Taiwan FDA registration 90edee4ff846c4627ba8de2f12b4ef9a
“Ivoclar Vivadent” TelioCAD for CEREC/inLab Blocks
TW: “義獲嘉偉瓦登特”特利歐喜瑞克取模用齒塊
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT AG·Registered Jul 13, 2018 – Jul 13, 2028ActiveRegistration details
- Analysis ID
- 90edee4ff846c4627ba8de2f12b4ef9a
- License Form
- Ministry of Health Medical Device Import No. 031294
- Customs Code
- DHA05603129406
Company information
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3770 Temporary crown and bridge resin
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 13, 2018
- Expiry Date
- Jul 13, 2028
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” TelioCAD for CEREC/inLab Blocks in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 90edee4ff846c4627ba8de2f12b4ef9a and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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