Taiwan FDA registration ed24d3e77dc0b94d7e5def022f6ed4a1
“Ivoclar Vivadent” IPS e.max CAD for PrograMill Blocks
TW: “義獲嘉偉瓦登特”易美普格蘭取模用齒塊
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT AG·Registered Apr 20, 2018 – Apr 20, 2028ActiveRegistration details
- Analysis ID
- ed24d3e77dc0b94d7e5def022f6ed4a1
- License Form
- Ministry of Health Medical Device Import No. 031045
- Customs Code
- DHA05603104501
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)
- F6660 Dental porcelain powder
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 20, 2018
- Expiry Date
- Apr 20, 2028
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” IPS e.max CAD for PrograMill Blocks in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed24d3e77dc0b94d7e5def022f6ed4a1 and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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