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Mobile X-ray system "Siemens" - Taiwan Registration e2a969975d7855cb9bff309cfdd05abb

Access comprehensive regulatory information for Mobile 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 e2a969975d7855cb9bff309cfdd05abb and manufactured by Siemens Healthcare GmbH, Advanced Therapies. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Siemens Healthineers AG, Advanced Therapies, Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., 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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e2a969975d7855cb9bff309cfdd05abb
Registration Details
Taiwan FDA Registration: e2a969975d7855cb9bff309cfdd05abb
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Device Details

Mobile X-ray system "Siemens"
TW: โ€œ่ฅฟ้–€ๅญโ€็งปๅ‹•ๅผXๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

e2a969975d7855cb9bff309cfdd05abb

DHAS9200106103

Company Information

Product Details

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

P Radiology Science

P.1730 ็…ง็›ธ้€่ฆ–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

Aug 14, 2019

Aug 14, 2024

Apr 15, 2020

Cancellation Information

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