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"Philips" magnetic resonance instrument - Taiwan Registration fea942a3e95ca5e09b52745393b67d29

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 fea942a3e95ca5e09b52745393b67d29 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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fea942a3e95ca5e09b52745393b67d29
Registration Details
Taiwan FDA Registration: fea942a3e95ca5e09b52745393b67d29
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Device Details

"Philips" magnetic resonance instrument
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€็ฃๅ…ฑๆŒฏๅ„€
Risk Class 2
Cancelled

Registration Details

fea942a3e95ca5e09b52745393b67d29

DHA00601925607

Company Information

Product Details

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

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

import

Dates and Status

Oct 06, 2008

Oct 06, 2018

Jul 15, 2022

Cancellation Information

Logged out

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