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"Siemens" magnetic resonance imaging instrument - Taiwan Registration 1ff1e8fe298c10718082f2492ab5c0c7

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 1ff1e8fe298c10718082f2492ab5c0c7 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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1ff1e8fe298c10718082f2492ab5c0c7
Registration Details
Taiwan FDA Registration: 1ff1e8fe298c10718082f2492ab5c0c7
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Device Details

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

Registration Details

1ff1e8fe298c10718082f2492ab5c0c7

DHA05602601702

Company Information

Product Details

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

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

Input;; 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.

Dates and Status

Mar 25, 2014

Mar 25, 2029

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