Taiwan FDA registration af1a3dc20ef43701660f5bc6cebca895
3M Filtek Supreme Flowable Restorative
TW: 3M流動性補牙材
Taiwan·Risk Class 2·MD·3M COMPANY 3M ESPE DENTAL PRODUCTS·Registered May 18, 2011 – May 18, 2026ExpiredRegistration details
- Analysis ID
- af1a3dc20ef43701660f5bc6cebca895
- License Form
- Department of Health Medical Device Import No. 022409
- Customs Code
- DHA00602240903
Company information
- Manufacturer
- 3M COMPANY 3M ESPE DENTAL PRODUCTS
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Minnesota Mining Manufacturing Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- May 18, 2011
- Expiry Date
- May 18, 2026
About this record
Access comprehensive regulatory information for 3M Filtek Supreme Flowable Restorative in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number af1a3dc20ef43701660f5bc6cebca895 and manufactured by 3M COMPANY 3M ESPE DENTAL PRODUCTS. The authorized representative in Taiwan is Taiwan Minnesota Mining Manufacturing Co., Ltd.
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