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"Siemens" magnetic resonance imaging instrument - Taiwan Registration 25d9d39c16a98a5e18c0983a2e97a80a

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 25d9d39c16a98a5e18c0983a2e97a80a 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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25d9d39c16a98a5e18c0983a2e97a80a
Registration Details
Taiwan FDA Registration: 25d9d39c16a98a5e18c0983a2e97a80a
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Device Details

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

Registration Details

25d9d39c16a98a5e18c0983a2e97a80a

DHA05602999403

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

Aug 01, 2017

Aug 01, 2027

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