Taiwan FDA registration a1ca767cdfda3e8d3847b4070d349a09

"Siemens" X-ray diagnostic system

TW: “西門子”X光診斷系統
Taiwan flagTaiwan·Risk Class 2·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; Siemens Healthcare GmbH, X-Ray Products (XP)·Registered Mar 10, 2014 – Mar 10, 2024Expired
Registration details
Analysis ID
a1ca767cdfda3e8d3847b4070d349a09
Customs Code
DHAS5602583701
Company information
Manufacturer Country
Germany;;China
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.1680 固定式X光系統
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
Mar 10, 2014
Expiry Date
Mar 10, 2024
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About this record

Access comprehensive regulatory information for "Siemens" X-ray diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a1ca767cdfda3e8d3847b4070d349a09 and manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; Siemens Healthcare GmbH, X-Ray Products (XP). The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT AX, and 3 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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