Taiwan FDA registration e18a5495fd4e5aa5be1e82b85ab25fcc
"Siemens" whole body diagnostic X-ray machine
TW: “西門子”全身診斷X光機
Taiwan·Risk Class 2·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.·Registered Nov 21, 2014 – Nov 21, 2019CancelledRegistration details
- Analysis ID
- e18a5495fd4e5aa5be1e82b85ab25fcc
- Customs Code
- DHAS9200063801
Company information
- Manufacturer
- SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.
- Manufacturer Country
- China
- 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;; Chinese goods;; 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 21, 2014
- Expiry Date
- Nov 21, 2019
- Cancellation Date
- Apr 10, 2020
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Siemens" whole body diagnostic X-ray machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e18a5495fd4e5aa5be1e82b85ab25fcc and manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.. The authorized representative in Taiwan is SIEMENS LIMITED.
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