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"Maximo" pulse oximetry - Taiwan Registration c7081a5feeb1ad86740a18999630ee55

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 c7081a5feeb1ad86740a18999630ee55 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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c7081a5feeb1ad86740a18999630ee55
Registration Details
Taiwan FDA Registration: c7081a5feeb1ad86740a18999630ee55
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Device Details

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

Registration Details

c7081a5feeb1ad86740a18999630ee55

DHA05602927102

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.2700.

Contract manufacturing;; input

Dates and Status

Jan 06, 2017

Jan 06, 2027

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