"Siemens" X-ray diagnostic system
- Analysis ID
- 806649eada1aa97d96524f48d9bde6d6
- Customs Code
- DHAS4200026508
- Manufacturer
- SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT AX
- Manufacturer Country
- Germany;;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
- Product Type (Level 2)
- P.1750 Computed tomography X-ray system;; P.1620 Continuous or intermittent fluoroscopic X-ray machine
- Import Information
- Input;; Chinese goods;; Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); Contract manufacturing;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
- Registration Date
- May 14, 2010
- Expiry Date
- May 14, 2015
- 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 806649eada1aa97d96524f48d9bde6d6 and manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT AX. 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 SHANGHAI MEDICAL EQUIPMENT LTD.;; Siemens Healthcare GmbH, X-Ray Products (XP), 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.