Taiwan FDA registration 2d79642e0f749d4dfbb80aa2f221e8cd

"Siemens" diagnostic X-ray tube sleeve assembly (unsterilized)

TW: "西門子" 診斷用X光球管套組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Siemens Healthineers AG, Advanced Therapies·Registered Jun 09, 2022 – Jun 09, 2027Active
Registration details
Analysis ID
2d79642e0f749d4dfbb80aa2f221e8cd
Customs Code
DHAS9402282805
Company information
Manufacturer Country
Germany
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
Limited to the first level identification range of the "X-ray tube sleeve assembly for diagnosis (P.1760)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1760 診斷用X光球管套組件
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); Input;; QMS/QSD
Dates and status
Registration Date
Jun 09, 2022
Expiry Date
Jun 09, 2027
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About this record

Access comprehensive regulatory information for "Siemens" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d79642e0f749d4dfbb80aa2f221e8cd and manufactured by Siemens Healthineers AG, Advanced Therapies. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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