Taiwan FDA registration 4f8445749aace2934afde65dbb49eb8c
“SDI” Stae Dentin/Enamel Single Component Total Etch Adhesive
TW: “斯蒂爾”史黛單劑式牙本質/琺瑯質全酸蝕黏著劑
Taiwan·Risk Class 2·MD·SDI Ltd·Registered Aug 14, 2021 – Aug 14, 2026ActiveRegistration details
- Analysis ID
- 4f8445749aace2934afde65dbb49eb8c
- License Form
- Ministry of Health Medical Device Import No. 034821
- Customs Code
- DHA05603482105
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)
- F3200 resin dental adhesive
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 14, 2021
- Expiry Date
- Aug 14, 2026
About this record
Access comprehensive regulatory information for “SDI” Stae Dentin/Enamel Single Component Total Etch Adhesive in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4f8445749aace2934afde65dbb49eb8c and manufactured by SDI Ltd. The authorized representative in Taiwan is FOMED BIOTECH INC..
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