Taiwan FDA registration cd0f18c0fdc2e11dfadbf7187e174431

"Singular" patient monitor

TW: “奇異”病患監視器
Taiwan flagTaiwan·Risk Class 2·Critikon De Mexico S. De R.L. De C.V.·Registered Jul 29, 2011 – Jul 29, 2026Expired
Registration details
Analysis ID
cd0f18c0fdc2e11dfadbf7187e174431
Customs Code
DHA00602265505
Company information
Manufacturer Country
Mexico
Authorized Representative
GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1025 Arrhythmia Detectors and Alerts
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Jul 29, 2011
Expiry Date
Jul 29, 2026
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About this record

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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