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"Philips" magnetic resonance imaging system - Taiwan Registration 27a37206f2c1df281a7f7e665be4bd0a

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 27a37206f2c1df281a7f7e665be4bd0a 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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27a37206f2c1df281a7f7e665be4bd0a
Registration Details
Taiwan FDA Registration: 27a37206f2c1df281a7f7e665be4bd0a
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Device Details

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

Registration Details

27a37206f2c1df281a7f7e665be4bd0a

DHA09200132707

Company Information

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

Input;; 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.

Dates and Status

Apr 11, 2022

Apr 11, 2027