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"Siemens" magnetic resonance imaging instrument - Taiwan Registration e170e7ecc8f0cd0a3c75e6802da9719f

Access comprehensive regulatory information for "Siemens" magnetic resonance imaging instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e170e7ecc8f0cd0a3c75e6802da9719f and manufactured by Siemens Healthineers AG, Magnetic Resonance (MR). 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, Magnetic Resonance (MR), SIEMENS SHENZHEN MAGNETIC RESONANCE LTD., 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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e170e7ecc8f0cd0a3c75e6802da9719f
Registration Details
Taiwan FDA Registration: e170e7ecc8f0cd0a3c75e6802da9719f
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Device Details

"Siemens" magnetic resonance imaging instrument
TW: โ€œ่ฅฟ้–€ๅญโ€็ฃๆŒฏ้€ ๅฝฑๅ„€
Risk Class 2

Registration Details

e170e7ecc8f0cd0a3c75e6802da9719f

DHA05603291800

Company Information

Product Details

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

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input

Dates and Status

Nov 09, 2019

Nov 09, 2029

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