Taiwan FDA registration f211710c3c6c68e64d959b4663e2ded1

The root canal of "Weier" is enlarged

TW: “葳爾”根管擴大材
Taiwan flagTaiwan·Risk Class 2·VERICOM CO., LTD.·Registered Oct 08, 2024 – Oct 08, 2029Active
Registration details
Analysis ID
f211710c3c6c68e64d959b4663e2ded1
Customs Code
DHA05603761902
Company information
Manufacturer
VERICOM CO., LTD.
Manufacturer Country
Korea, Republic of
Authorized Representative
SUNDENT CORPORATION
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.3820 根管充填樹脂
Import Information
import
Dates and status
Registration Date
Oct 08, 2024
Expiry Date
Oct 08, 2029
About this record

Access comprehensive regulatory information for The root canal of "Weier" is enlarged in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f211710c3c6c68e64d959b4663e2ded1 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.

Free DatabasePowered by Pure Global AI89,000+ Devices