Taiwan FDA registration 46818f436601d3842e00022789b77522
"Yi Yue Jia Wei Wadent" double cross-linked resin denture
TW: “義獲嘉偉瓦登特”雙交聯樹脂義齒
Registration details
- Analysis ID
- 46818f436601d3842e00022789b77522
- Customs Code
- DHA05603319705
Company information
- Manufacturer Country
- Italy;;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 Dentistry
- Product Type (Level 2)
- F.3590 成型塑膠假牙床
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Feb 15, 2020
- Expiry Date
- Feb 15, 2030
About this record
Access comprehensive regulatory information for "Yi Yue Jia Wei Wadent" double cross-linked resin denture in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46818f436601d3842e00022789b77522 and manufactured by Ivoclar Vivadent Manufacturing GmbH;;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