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“Aulisa"Infant Oximeter Module - Taiwan Registration 5113025f1d41dcd32b8c1fec717f23a9

Access comprehensive regulatory information for “Aulisa"Infant Oximeter Module in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5113025f1d41dcd32b8c1fec717f23a9 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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5113025f1d41dcd32b8c1fec717f23a9
Registration Details
Taiwan FDA Registration: 5113025f1d41dcd32b8c1fec717f23a9
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Device Details

“Aulisa"Infant Oximeter Module
TW: “安麗莎"嬰兒血氧模組
Risk Class 2
MD

Registration Details

5113025f1d41dcd32b8c1fec717f23a9

Ministry of Health Medical Device Manufacturing No. 007452

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E2700 Oximeter

Produced in Taiwan, China

Dates and Status

Apr 03, 2022

Apr 03, 2027