Pure Global

“Vortran” GO2VENT - Taiwan Registration e1d65413ff551c0720ef8493117b5a35

Access comprehensive regulatory information for “Vortran” GO2VENT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1d65413ff551c0720ef8493117b5a35 and manufactured by VORTRAN MEDICAL TECHNOLOGY 1, INC.. The authorized representative in Taiwan is HI-CLEARANCE INC..

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
e1d65413ff551c0720ef8493117b5a35
Registration Details
Taiwan FDA Registration: e1d65413ff551c0720ef8493117b5a35
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Vortran” GO2VENT
TW: “福全” 自動復甦器
Risk Class 2
MD

Registration Details

e1d65413ff551c0720ef8493117b5a35

Ministry of Health Medical Device Import No. 036379

DHA05603637900

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology

D5925 Powered Emergency Respirator

Imported from abroad

Dates and Status

Jun 14, 2023

Jun 14, 2028