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"Siemens" magnetic resonance imaging system - Taiwan Registration 3b24aa95add9e553ef30ca1ac1815860

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 3b24aa95add9e553ef30ca1ac1815860 and manufactured by SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.. 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 Healthineers AG, Magnetic Resonance (MR), 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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3b24aa95add9e553ef30ca1ac1815860
Registration Details
Taiwan FDA Registration: 3b24aa95add9e553ef30ca1ac1815860
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Device Details

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

Registration Details

3b24aa95add9e553ef30ca1ac1815860

DHA09200076309

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". Chinese goods;; input

Dates and Status

May 13, 2016

May 13, 2021

Aug 04, 2023

Cancellation Information

Logged out

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