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"Singular" patient monitor - Taiwan Registration cd0f18c0fdc2e11dfadbf7187e174431

Access comprehensive regulatory information for "Singular" patient monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cd0f18c0fdc2e11dfadbf7187e174431 and manufactured by Critikon De Mexico S. De R.L. De C.V.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GE HEALTHCARE FINLAND OY, and 1 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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cd0f18c0fdc2e11dfadbf7187e174431
Registration Details
Taiwan FDA Registration: cd0f18c0fdc2e11dfadbf7187e174431
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Device Details

"Singular" patient monitor
TW: โ€œๅฅ‡็•ฐโ€็—…ๆ‚ฃ็›ฃ่ฆ–ๅ™จ
Risk Class 2

Registration Details

cd0f18c0fdc2e11dfadbf7187e174431

DHA00602265505

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1025 Arrhythmia Detectors and Alerts

Contract manufacturing;; input

Dates and Status

Jul 29, 2011

Jul 29, 2026

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