Taiwan FDA registration 971835cc98d26625f6799f9c494a96ca
"Siemens" X-ray system for diagnosis and treatment in urology
TW: "西門子" 泌尿科診斷及治療專用X光系統
Taiwan·Risk Class 2·SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP·Registered Nov 18, 2005 – Nov 18, 2020CancelledRegistration details
- Analysis ID
- 971835cc98d26625f6799f9c494a96ca
- Customs Code
- DHAS0601356205
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
- Nov 18, 2005
- Expiry Date
- Nov 18, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Siemens" X-ray system for diagnosis and treatment in urology in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 971835cc98d26625f6799f9c494a96ca and manufactured by SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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