“DenFil N” Light-cured restorative nano hybrid composite resin - Taiwan Registration e333a2a58c862a12117cef147fd2f1ed
Access comprehensive regulatory information for “DenFil N” Light-cured restorative nano hybrid composite resin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e333a2a58c862a12117cef147fd2f1ed and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.
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
e333a2a58c862a12117cef147fd2f1ed
Ministry of Health Medical Device Import No. 030968
DHA05603096802
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
Mar 15, 2018
Mar 15, 2028

