Taiwan FDA registration 98fbc214e97e70dc79d4dc18fb4ba9e2
3M ESPE Filtek Bulk Fill Posterior Restorative
TW: 3M菲特波克齒體填充後牙復形材料
Taiwan·Risk Class 2·MD·3M ESPE DENTAL PRODUCTS·Registered May 04, 2015 – May 04, 2025ExpiredRegistration details
- Analysis ID
- 98fbc214e97e70dc79d4dc18fb4ba9e2
- License Form
- Ministry of Health Medical Device Import No. 027378
- Customs Code
- DHA05602737800
Company information
- Manufacturer
- 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 04, 2015
- Expiry Date
- May 04, 2025
About this record
Access comprehensive regulatory information for 3M ESPE Filtek Bulk Fill Posterior Restorative in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98fbc214e97e70dc79d4dc18fb4ba9e2 and manufactured by 3M ESPE DENTAL PRODUCTS. The authorized representative in Taiwan is Taiwan Minnesota Mining Manufacturing Co., Ltd.
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