Taiwan FDA registration 5179680f799445f377405dad23172b7e

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

TW: “西門子”診斷用X光球管套組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.·Registered Jul 30, 2008 – Jul 30, 2018Cancelled
Registration details
Analysis ID
5179680f799445f377405dad23172b7e
Customs Code
DHAS4600055102
Company information
Manufacturer Country
China
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
Limited to the first-level identification range of the Measures for the Administration of Medical Devices "X-ray Tube Sleeve Components for Diagnosis (P.1760)".
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); Chinese goods;; input
Dates and status
Registration Date
Jul 30, 2008
Expiry Date
Jul 30, 2018
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for X-ray tube sleeve assembly for diagnostic "Siemens" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5179680f799445f377405dad23172b7e and manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including SIEMENS HEALTHCARE GMBH, ADVANCED THERAPIES, Siemens Healthcare GmbH, and 5 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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