Taiwan FDA registration 49a314cb7e2f8e353b46ab82e5ddae1f
“SDI” Aura eASY Ultra Universal Restorative Material
TW: “斯蒂爾”歐拉易通用型樹脂補牙材
Taiwan·Risk Class 2·MD·SDI Ltd·Registered Dec 09, 2021 – Dec 09, 2026ActiveRegistration details
- Analysis ID
- 49a314cb7e2f8e353b46ab82e5ddae1f
- License Form
- Ministry of Health Medical Device Import No. 035084
- Customs Code
- DHA05603508402
Company information
- Manufacturer
- SDI Ltd
- Manufacturer Country
- Australia
- Authorized Representative
- FOMED BIOTECH INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 09, 2021
- Expiry Date
- Dec 09, 2026
About this record
Access comprehensive regulatory information for “SDI” Aura eASY Ultra Universal Restorative Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49a314cb7e2f8e353b46ab82e5ddae1f and manufactured by SDI Ltd. The authorized representative in Taiwan is FOMED BIOTECH INC..
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