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"Philips" magnetic resonance imaging system software - Taiwan Registration 74b43adcf2efc3ae8c8b1112317c793f

Access comprehensive regulatory information for "Philips" magnetic resonance imaging system software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 74b43adcf2efc3ae8c8b1112317c793f and manufactured by Philips DS North America LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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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74b43adcf2efc3ae8c8b1112317c793f
Registration Details
Taiwan FDA Registration: 74b43adcf2efc3ae8c8b1112317c793f
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Device Details

"Philips" magnetic resonance imaging system software
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€็ฃๆŒฏๅฝฑๅƒ็ณป็ตฑ่ปŸ้ซ”
Risk Class 2

Registration Details

74b43adcf2efc3ae8c8b1112317c793f

DHA00602230504

Company Information

United States

Product Details

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

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

Input;; Contract manufacturing

Dates and Status

May 07, 2011

May 07, 2026