"Siemens" ultrasonic system
Taiwan·Risk Class 2·SIEMENS MEDICAL SOLUTIONS USA, INC.·Registered Jul 11, 2008 – Jul 11, 2013Cancelled- Analysis ID
- ee7be885b64bd63cd959bbd796eff109
- Customs Code
- DHA00601910907
- Manufacturer
- SIEMENS MEDICAL SOLUTIONS USA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS 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
- Jul 11, 2008
- Expiry Date
- Jul 11, 2013
- Cancellation Date
- Aug 10, 2015
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Siemens" ultrasonic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee7be885b64bd63cd959bbd796eff109 and manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.. The authorized representative in Taiwan is SIEMENS LIMITED.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Siemens Medical Solutions USA, Inc.;; Siemens Healthcare s.r.o., SIEMENS MEDICAL SOLUTIONS USA, INC. ULTRASOUND DIVISION, 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.