Taiwan FDA registration ac0f63a87975921da8cd28eb62a48f03

“DENMAT” FLASH LITE

TW: “登美”光固化機
Taiwan flagTaiwan·Risk Class 2·MD·DEN-MAT HOLDINGS, LLC·Registered Oct 16, 2017 – Oct 16, 2027Active
Registration details
Analysis ID
ac0f63a87975921da8cd28eb62a48f03
License Form
Ministry of Health Medical Device Import No. 030348
Customs Code
DHA05603034801
Company information
Manufacturer Country
United States
Authorized Representative
AIREX CORP.
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)
F6070 UV activator for polymerization
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 16, 2017
Expiry Date
Oct 16, 2027
About this record

Access comprehensive regulatory information for “DENMAT” FLASH LITE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ac0f63a87975921da8cd28eb62a48f03 and manufactured by DEN-MAT HOLDINGS, LLC. The authorized representative in Taiwan is AIREX CORP..

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