Taiwan FDA registration 7a1e7c0ac47b5f8a51ce9b2b845e0d7d
“SDI” Aura Easyflow Ultra Universal Restorative Material
TW: “斯蒂爾”歐拉流動性通用型樹脂補牙材
Taiwan·Risk Class 2·MD·SDI Ltd·Registered Dec 09, 2021 – Dec 09, 2026ActiveRegistration details
- Analysis ID
- 7a1e7c0ac47b5f8a51ce9b2b845e0d7d
- License Form
- Ministry of Health Medical Device Import No. 035083
- Customs Code
- DHA05603508300
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 Easyflow 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 7a1e7c0ac47b5f8a51ce9b2b845e0d7d and manufactured by SDI Ltd. The authorized representative in Taiwan is FOMED BIOTECH INC..
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