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"Philips" magnetic resonance instrument - Taiwan Registration 26fd8c5897b906a8820e054ab19eb509

Access comprehensive regulatory information for "Philips" magnetic resonance instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 26fd8c5897b906a8820e054ab19eb509 and manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., 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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26fd8c5897b906a8820e054ab19eb509
Registration Details
Taiwan FDA Registration: 26fd8c5897b906a8820e054ab19eb509
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Device Details

"Philips" magnetic resonance instrument
TW: "้ฃ›ๅˆฉๆตฆ" ็ฃๅ…ฑๆŒฏๅ„€
Risk Class 2

Registration Details

26fd8c5897b906a8820e054ab19eb509

DHA00601049200

Company Information

Product Details

P Radiology Science

import

Dates and Status

Dec 26, 2003

Dec 26, 2028

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