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"Canon" magnetic resonance diagnostic device - Taiwan Registration 0f3f3d3345fde8e45c84c87c448fa593

Access comprehensive regulatory information for "Canon" magnetic resonance diagnostic device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f3f3d3345fde8e45c84c87c448fa593 and manufactured by Canon Medical Systems Corporation. The authorized representative in Taiwan is ROTARY TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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0f3f3d3345fde8e45c84c87c448fa593
Registration Details
Taiwan FDA Registration: 0f3f3d3345fde8e45c84c87c448fa593
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Device Details

"Canon" magnetic resonance diagnostic device
TW: โ€œไฝณ่ƒฝโ€็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ
Risk Class 2

Registration Details

0f3f3d3345fde8e45c84c87c448fa593

DHA05602773903

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

Sep 17, 2015

Sep 17, 2025