Taiwan FDA registration 15e6598f86998e240f0c080df83255d0
Digital diagnostic X-ray system "Siemens"
TW: “西門子”數位式診斷X光系統
Taiwan·Risk Class 2·SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP·Registered Mar 14, 2007 – Mar 14, 2017CancelledRegistration details
- Analysis ID
- 15e6598f86998e240f0c080df83255d0
- Customs Code
- DHAS0601781209
Company information
- Manufacturer
- SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP
- Manufacturer Country
- Germany
- Authorized Representative
- SIEMENS HEALTHCARE 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.1650 透視X光影像增感管
- 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
- Mar 14, 2007
- Expiry Date
- Mar 14, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Digital diagnostic X-ray system "Siemens" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 15e6598f86998e240f0c080df83255d0 and manufactured by SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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