"Singular" ultrasound diagnostic system
- Analysis ID
- 746d88cd91e88ba3cfb754da2d91d923
- Customs Code
- DHA00601772700
- Manufacturer
- GE HEALTHCARE AUSTRIA GMBH & CO OG
- Manufacturer Country
- Austria
- Authorized Representative
- GE MEDICAL SYSTEMS TAIWAN, LTD.
- Intended Use
- For details, please refer to the approved version of Chinese copy
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- import
- Registration Date
- Jan 26, 2007
- Expiry Date
- Jan 26, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Singular" ultrasound diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 746d88cd91e88ba3cfb754da2d91d923 and manufactured by GE HEALTHCARE AUSTRIA GMBH & CO OG. 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 AUSTRIA GMBH & CO OG, 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.