Pure Global

“DENMAT” FLASH LITE - Taiwan Registration ac0f63a87975921da8cd28eb62a48f03

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 Database
Powered by Pure Global AI
89,000+ Devices
ac0f63a87975921da8cd28eb62a48f03
Registration Details
Taiwan FDA Registration: ac0f63a87975921da8cd28eb62a48f03
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“DENMAT” FLASH LITE
TW: “登美”光固化機
Risk Class 2
MD

Registration Details

ac0f63a87975921da8cd28eb62a48f03

Ministry of Health Medical Device Import No. 030348

DHA05603034801

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F6070 UV activator for polymerization

Imported from abroad

Dates and Status

Oct 16, 2017

Oct 16, 2027