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"Maximo" pulse oximetry - Taiwan Registration 8dd0f26d5368b160fa40168f568dddb7

Access comprehensive regulatory information for "Maximo" pulse oximetry in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8dd0f26d5368b160fa40168f568dddb7 and manufactured by Masimo Corporation;;Industrial Vallera de Mexicali, S.A. de C.V.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Masimo Corporation;;Industrial Vallera de Mexicali, S.A. de C.V., and 2 recent registrations in the same category. 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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8dd0f26d5368b160fa40168f568dddb7
Registration Details
Taiwan FDA Registration: 8dd0f26d5368b160fa40168f568dddb7
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Device Details

"Maximo" pulse oximetry
TW: โ€œ้‚ๅฟƒ่ซพโ€ ่„ˆๆ่ก€ๆฐงๆฟƒๅบฆๆธฌๅฎšๅ„€
Risk Class 2

Registration Details

8dd0f26d5368b160fa40168f568dddb7

DHA05603677508

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.2700.

Input;; Contract manufacturing

Dates and Status

Dec 03, 2023

Dec 03, 2028

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