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"Siemens" magnetic resonance imaging system - Taiwan Registration b3806b15dfc760a70ea36bbb6e3f3fa0

Access comprehensive regulatory information for "Siemens" magnetic resonance imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b3806b15dfc760a70ea36bbb6e3f3fa0 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, 1 companies making similar products including SIEMENS SHENZHEN MAGNETIC RESONANCE LTD., and 1 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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b3806b15dfc760a70ea36bbb6e3f3fa0
Registration Details
Taiwan FDA Registration: b3806b15dfc760a70ea36bbb6e3f3fa0
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Device Details

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

Registration Details

b3806b15dfc760a70ea36bbb6e3f3fa0

DHA05603280602

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

Aug 29, 2019

Aug 29, 2029

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