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“Aulisa”Combo Monitoring System - Taiwan Registration 69b474090388824525a3d3077ec6b597

Access comprehensive regulatory information for “Aulisa”Combo 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 69b474090388824525a3d3077ec6b597 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.

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69b474090388824525a3d3077ec6b597
Registration Details
Taiwan FDA Registration: 69b474090388824525a3d3077ec6b597
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Device Details

“Aulisa”Combo Monitoring System
TW: “安麗莎”多功能監控系統
Risk Class 2
MD

Registration Details

69b474090388824525a3d3077ec6b597

Ministry of Health Medical Device Manufacturing No. 007782

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

Dec 16, 2022

Dec 16, 2027