Taiwan FDA registration 6ebcbc477de9ab2a12abb70e2cf402be
“Ivoclar Vivadent” IPS e.max CAD for KaVo ARCTICA
TW: “義獲嘉偉瓦登特”阿堤卡齒雕機易美瓷塊
Taiwan·Risk Class 2·MD·IVOCLAR VIVADENT AG·Registered Oct 17, 2017 – Oct 17, 2022CancelledRegistration details
- Analysis ID
- 6ebcbc477de9ab2a12abb70e2cf402be
- License Form
- Ministry of Health Medical Device Import No. 030350
- Customs Code
- DHA05603035001
Company information
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- MYWAY INTERNATIONAL CO., LTD.
Product details
- 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
- Oct 17, 2017
- Expiry Date
- Oct 17, 2022
- Cancellation Date
- Feb 27, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” IPS e.max CAD for KaVo ARCTICA in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ebcbc477de9ab2a12abb70e2cf402be and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is MYWAY INTERNATIONAL CO., LTD..
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