Taiwan FDA registration 6b7d1e7c132502d55d829dffb4157dc8
Mobile fluoroscopic X-ray system "Siemens"
TW: “西門子”移動式透視X光系統
Taiwan·Risk Class 2·Siemens Healthineers AG, Advanced Therapies·Registered Mar 07, 2019 – Mar 07, 2029ActiveRegistration details
- Analysis ID
- 6b7d1e7c132502d55d829dffb4157dc8
- Customs Code
- DHAS5603228403
Company information
- Manufacturer
- Siemens Healthineers AG, Advanced Therapies
- Manufacturer Country
- Germany
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Cios Spin The following blanks
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1650 透視X光影像增感管
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
- Registration Date
- Mar 07, 2019
- Expiry Date
- Mar 07, 2029
About this record
Access comprehensive regulatory information for Mobile fluoroscopic 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 6b7d1e7c132502d55d829dffb4157dc8 and manufactured by Siemens Healthineers AG, Advanced Therapies. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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