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"Philips" magnetic resonance imaging system - Taiwan Registration c876420d35565e5d5e9de860ffe271b6

Access comprehensive regulatory information for "Philips" 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 c876420d35565e5d5e9de860ffe271b6 and manufactured by Philips Healthcare (Suzhou) Co., Ltd. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Philips Medical Systems Nederland B.V., PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., and 5 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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c876420d35565e5d5e9de860ffe271b6
Registration Details
Taiwan FDA Registration: c876420d35565e5d5e9de860ffe271b6
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Device Details

"Philips" magnetic resonance imaging system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€็ฃๆŒฏ้€ ๅฝฑ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

c876420d35565e5d5e9de860ffe271b6

DHA09200071307

Company Information

Product Details

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

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

Chinese goods;; 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

Nov 11, 2015

Nov 11, 2020

Jul 15, 2022

Cancellation Information

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