Taiwan FDA registration fcd3b4d7d6fc21c93f769e880a095cd5
“SDI” Set PP Self Etching, Self Adhesive Resin Cement
TW: “斯蒂爾”希爾特自蝕自黏樹脂黏合劑
Registration details
- Analysis ID
- fcd3b4d7d6fc21c93f769e880a095cd5
- License Form
- Ministry of Health Medical Device Import No. 034936
- Customs Code
- DHA05603493609
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)
- F3275 Dental cement (Sminting)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 02, 2021
- Expiry Date
- Sep 02, 2026
About this record
Access comprehensive regulatory information for “SDI” Set PP Self Etching, Self Adhesive Resin Cement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fcd3b4d7d6fc21c93f769e880a095cd5 and manufactured by SDI Ltd. The authorized representative in Taiwan is FOMED BIOTECH INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices