“Spacer” Light-curing temporary filling material - Taiwan Registration df8cb4bbd27606258d85b804a7a1026a
Access comprehensive regulatory information for “Spacer” Light-curing temporary filling material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df8cb4bbd27606258d85b804a7a1026a 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
df8cb4bbd27606258d85b804a7a1026a
Ministry of Health Medical Device Import No. 031595
DHA05603159507
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
Sep 07, 2018
Sep 07, 2028

