"Siemens" ultrasonic diagnostic system
Taiwan·Risk Class 2·PANASONIC HEALTHCARE CO., LTD.·Registered Mar 26, 2007 – Mar 26, 2017Cancelled- Analysis ID
- 21a9594e55aa9b984e165099c9bb5869
- Customs Code
- DHA00601795701
- Manufacturer
- PANASONIC HEALTHCARE CO., LTD.
- Manufacturer Country
- Japan
- 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
- Mar 26, 2007
- Expiry Date
- Mar 26, 2017
- Cancellation Date
- Nov 04, 2019
- 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 21a9594e55aa9b984e165099c9bb5869 and manufactured by PANASONIC HEALTHCARE CO., LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including SIEMENS MEDICAL SOLUTIONS USA, INC., PANASONIC HEALTHCARE CO., LTD., 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.