Taiwan FDA registration 72a008baa9de87f5b738beb163f1cb93
“SDI” Aura Ultra Universal Restorative Material
TW: “斯蒂爾”歐拉通用型樹脂補牙材
Taiwan·Risk Class 2·MD·SDI Ltd·Registered Dec 11, 2021 – Dec 11, 2026ActiveRegistration details
- Analysis ID
- 72a008baa9de87f5b738beb163f1cb93
- License Form
- Ministry of Health Medical Device Import No. 035088
- Customs Code
- DHA05603508800
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 11, 2021
- Expiry Date
- Dec 11, 2026
About this record
Access comprehensive regulatory information for “SDI” Aura 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 72a008baa9de87f5b738beb163f1cb93 and manufactured by SDI Ltd. The authorized representative in Taiwan is FOMED BIOTECH INC..
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