Taiwan FDA registration 96fa5a76365732332701dc84aa652e9a
“SDI” Wave Flowable Releasing Composite
TW: “斯蒂爾”維夫流動性樹脂補牙材
Taiwan·Risk Class 2·MD·SDI Ltd·Registered Oct 22, 2021 – Oct 22, 2026ActiveRegistration details
- Analysis ID
- 96fa5a76365732332701dc84aa652e9a
- License Form
- Ministry of Health Medical Device Import No. 034979
- Customs Code
- DHA05603497901
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 Dental devices
- Product Type (Level 2)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 22, 2021
- Expiry Date
- Oct 22, 2026
About this record
Access comprehensive regulatory information for “SDI” Wave Flowable Releasing Composite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 96fa5a76365732332701dc84aa652e9a and manufactured by SDI Ltd. The authorized representative in Taiwan is FOMED BIOTECH INC..
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