Taiwan FDA registration 4c50013cb3936b805857a99f8465cccb
“SDI” Aura Bulk Fill Universal Restorative Material
TW: “斯蒂爾”歐拉巴克通用型樹脂補牙材
Taiwan·Risk Class 2·MD·SDI Ltd·Registered Dec 16, 2021 – Dec 16, 2026ActiveRegistration details
- Analysis ID
- 4c50013cb3936b805857a99f8465cccb
- License Form
- Ministry of Health Medical Device Import No. 035095
- Customs Code
- DHA05603509507
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 16, 2021
- Expiry Date
- Dec 16, 2026
About this record
Access comprehensive regulatory information for “SDI” Aura Bulk Fill 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 4c50013cb3936b805857a99f8465cccb and manufactured by SDI Ltd. The authorized representative in Taiwan is FOMED BIOTECH INC..
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