Taiwan FDA registration ce4aea3fdbfa0eb30aaf9e99a1bac1d1
“Ivoclar Vivadent” Tetric CAD for CEREC/ inLab Blocks
TW: “義獲嘉偉瓦登特”德崔立喜瑞克取模用齒塊
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT AG·Registered Feb 15, 2020 – Feb 15, 2025ExpiredRegistration details
- Analysis ID
- ce4aea3fdbfa0eb30aaf9e99a1bac1d1
- License Form
- Ministry of Health Medical Device Import No. 033198
- Customs Code
- DHA05603319807
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)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 15, 2020
- Expiry Date
- Feb 15, 2025
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” Tetric CAD 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 ce4aea3fdbfa0eb30aaf9e99a1bac1d1 and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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