Taiwan FDA registration f3483bda59536ea2a96b84193b14b1e0
3M Filtek Z350 XT Universal Restorative
TW: 3M 前後牙通用複合樹脂補牙材
Taiwan·Risk Class 2·MD·3M COMPANY 3M ESPE DENTAL PRODUCTS·Registered Mar 12, 2010 – Mar 12, 2025ExpiredRegistration details
- Analysis ID
- f3483bda59536ea2a96b84193b14b1e0
- License Form
- Department of Health Medical Device Import No. 020662
- Customs Code
- DHA00602066205
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
- Mar 12, 2010
- Expiry Date
- Mar 12, 2025
About this record
Access comprehensive regulatory information for 3M Filtek Z350 XT Universal Restorative in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3483bda59536ea2a96b84193b14b1e0 and manufactured by 3M COMPANY 3M ESPE DENTAL PRODUCTS. The authorized representative in Taiwan is Taiwan Minnesota Mining Manufacturing Co., Ltd.
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