"Siemens" X-ray diagnostic system
Taiwan·Risk Class 2·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.·Registered Mar 17, 2006 – Mar 17, 2016Cancelled- Analysis ID
- b978b07808d4166b32ad694a1293d295
- Customs Code
- DHAS4200010002
- Manufacturer
- SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.
- Manufacturer Country
- China
- Authorized Representative
- SIEMENS LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Import Information
- Chinese goods;; Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
- Registration Date
- Mar 17, 2006
- Expiry Date
- Mar 17, 2016
- Cancellation Date
- Jul 31, 2018
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Siemens" X-ray 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 b978b07808d4166b32ad694a1293d295 and manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.. The authorized representative in Taiwan is SIEMENS LIMITED.
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; Siemens Healthcare GmbH, X-Ray Products (XP), SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT AX, 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.