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“Aulisa”Oximeter Module - Taiwan Registration f6b4115f22a6e146fc3f8d1953d7a208

Access comprehensive regulatory information for “Aulisa”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 f6b4115f22a6e146fc3f8d1953d7a208 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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f6b4115f22a6e146fc3f8d1953d7a208
Registration Details
Taiwan FDA Registration: f6b4115f22a6e146fc3f8d1953d7a208
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Device Details

“Aulisa”Oximeter Module
TW: “安麗莎”血氧模組
Risk Class 2
MD

Registration Details

f6b4115f22a6e146fc3f8d1953d7a208

Ministry of Health Medical Device Manufacturing No. 007660

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

Jul 16, 2022

Jul 16, 2027