Pure Global

“Aulisa” Multiple Patient Digital Vital Sign Monitoring System - Taiwan Registration 84dee1c3006469d5210f2a076eb91dcc

Access comprehensive regulatory information for “Aulisa” Multiple Patient Digital Vital Sign Monitoring System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84dee1c3006469d5210f2a076eb91dcc and manufactured by TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC.. The authorized representative in Taiwan is TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, 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
84dee1c3006469d5210f2a076eb91dcc
Registration Details
Taiwan FDA Registration: 84dee1c3006469d5210f2a076eb91dcc
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Aulisa” Multiple Patient Digital Vital Sign Monitoring System
TW: “安麗莎” 中央生理訊號監控系統軟體
Risk Class 2
MD

Registration Details

84dee1c3006469d5210f2a076eb91dcc

Ministry of Health Medical Device Manufacturing No. 007465

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E2300 Cardiac Monitor (incl. Cardiac Counter and Heart Rate Alert)

Produced in Taiwan, China

Dates and Status

May 08, 2022

May 08, 2027