"Siemens" ultrasonic diagnostic system
Taiwan·Risk Class 2·SIEMENS MEDICAL SOLUTIONS USA, INC.·Registered May 24, 2012 – May 24, 2022Cancelled- Analysis ID
- 121d77a1c6b93b9438ce4819040fe5d3
- Customs Code
- DHA00602351303
- Manufacturer
- SIEMENS MEDICAL SOLUTIONS USA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- 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
- May 24, 2012
- Expiry Date
- May 24, 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 "Siemens" ultrasonic 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 121d77a1c6b93b9438ce4819040fe5d3 and manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including PANASONIC HEALTHCARE CO., LTD., Siemens Medical Solutions USA, Inc., and 3 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.