"Singular" patient monitor
- Analysis ID
- cd0f18c0fdc2e11dfadbf7187e174431
- Customs Code
- DHA00602265505
- Manufacturer
- Critikon De Mexico S. De R.L. De C.V.
- Manufacturer Country
- Mexico
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
- 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
- Registration Date
- Jul 29, 2011
- Expiry Date
- Jul 29, 2026
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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.