"Singular" ultrasound system
Taiwan·Risk Class 2·GE Medical Systems Imformation Technologies – Critikon De Mexico S. De R.L. De C.V.;; GE Medical Systems Ultrasound & Primary Care Diagnostics LLC·Registered Dec 21, 2018 – Dec 21, 2028Active- Analysis ID
- c31e37127a9f1ce7a257d5465ce4d813
- Customs Code
- DHA05603187500
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- import
- Registration Date
- Dec 21, 2018
- Expiry Date
- Dec 21, 2028
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Access comprehensive regulatory information for "Singular" ultrasound system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c31e37127a9f1ce7a257d5465ce4d813 and manufactured by GE Medical Systems Imformation Technologies – Critikon De Mexico S. De R.L. De C.V.;; GE Medical Systems Ultrasound & Primary Care Diagnostics LLC. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including WIPRO GE HEALTHCARE PVT. LTD., GE VINGMED ULTRASOUND AS, and 5 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.