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"Siemens" X-ray diagnostic system - Taiwan Registration a1ca767cdfda3e8d3847b4070d349a09

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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a1ca767cdfda3e8d3847b4070d349a09
Registration Details
Taiwan FDA Registration: a1ca767cdfda3e8d3847b4070d349a09
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Device Details

"Siemens" X-ray diagnostic system
TW: โ€œ่ฅฟ้–€ๅญโ€Xๅ…‰่จบๆ–ท็ณป็ตฑ
Risk Class 2

Registration Details

a1ca767cdfda3e8d3847b4070d349a09

DHAS5602583701

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Mar 10, 2014

Mar 10, 2024