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Mobile X-ray system "Siemens" - Taiwan Registration 57e02ec388cae6145726cc8392ff77ad

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 57e02ec388cae6145726cc8392ff77ad 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, 3 companies making similar products including Siemens Healthineers AG, Advanced Therapies, Siemens Healthcare GmbH, Advanced Therapies, 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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57e02ec388cae6145726cc8392ff77ad
Registration Details
Taiwan FDA Registration: 57e02ec388cae6145726cc8392ff77ad
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Device Details

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

Registration Details

57e02ec388cae6145726cc8392ff77ad

DHAS5603322403

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

Jan 20, 2020

Aug 14, 2029