3M ESPE Filtek Bulk Fill Posterior Restorative - Taiwan Registration 98fbc214e97e70dc79d4dc18fb4ba9e2
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.
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.
Device Details
Registration Details
98fbc214e97e70dc79d4dc18fb4ba9e2
Ministry of Health Medical Device Import No. 027378
DHA05602737800
Product Details
For details, it is Chinese approved copy of the imitation order
F Dental devices
F3690 Resin tusk wood
Imported from abroad
Dates and Status
May 04, 2015
May 04, 2025

