Taiwan FDA registration 7e2a4b2673c7e61f166655118fc5fe13
"Siemens" digital X-ray system
TW: “西門子”數位X光系統
Taiwan·Risk Class 2·SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP·Registered Nov 04, 2010 – Nov 04, 2015CancelledRegistration details
- Analysis ID
- 7e2a4b2673c7e61f166655118fc5fe13
- Customs Code
- DHAS0602163808
Company information
- Manufacturer
- SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP
- Manufacturer Country
- Germany
- Authorized Representative
- SIEMENS LIMITED
Product details
- 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.1680 固定式X光系統
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Nov 04, 2010
- Expiry Date
- Nov 04, 2015
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Siemens" digital X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e2a4b2673c7e61f166655118fc5fe13 and manufactured by SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP. The authorized representative in Taiwan is SIEMENS LIMITED.
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