Taiwan FDA registration 4ffacf803591c961c2b4b50f47cf719c
"Yi Ke Jia Wei Wadent" dental alloy
TW: "義獲嘉偉瓦登特"牙科用合金
Taiwan·Risk Class 2·IVOCLAR VIVADENT, INC.·Registered Jan 29, 2007 – Jan 29, 2012CancelledRegistration details
- Analysis ID
- 4ffacf803591c961c2b4b50f47cf719c
- Customs Code
- DHA00601773203
Company information
- Manufacturer
- IVOCLAR VIVADENT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TEI JEL ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3060 Dentistry uses gold-based alloys and precious metal-based alloys
- Import Information
- import
Dates and status
- Registration Date
- Jan 29, 2007
- Expiry Date
- Jan 29, 2012
- Cancellation Date
- Apr 03, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Yi Ke Jia Wei Wadent" dental alloy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ffacf803591c961c2b4b50f47cf719c and manufactured by IVOCLAR VIVADENT, INC.. The authorized representative in Taiwan is TEI JEL ENTERPRISE CO., LTD..
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