Pure Global

“UPOC"Fingertip Pulse Oximeter - Taiwan Registration 0980fa54351a6952a6bbee0e5a8f7baf

Access comprehensive regulatory information for “UPOC"Fingertip Pulse Oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0980fa54351a6952a6bbee0e5a8f7baf and manufactured by Faciox Inc.. The authorized representative in Taiwan is Faciox 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
0980fa54351a6952a6bbee0e5a8f7baf
Registration Details
Taiwan FDA Registration: 0980fa54351a6952a6bbee0e5a8f7baf
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“UPOC"Fingertip Pulse Oximeter
TW: “怡氧"指夾式脈搏血氧儀
Risk Class 2
MD

Registration Details

0980fa54351a6952a6bbee0e5a8f7baf

Ministry of Health Medical Device Manufacturing No. 007825

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E2700 Oximeter

Produced in Taiwan, China

Dates and Status

Mar 11, 2023

Mar 11, 2028