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"Philips" magnetic resonance imaging system - Taiwan Registration d018a1b75ae97f09423ac1f97b3e25d6

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 d018a1b75ae97f09423ac1f97b3e25d6 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, 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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d018a1b75ae97f09423ac1f97b3e25d6
Registration Details
Taiwan FDA Registration: d018a1b75ae97f09423ac1f97b3e25d6
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Device Details

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

Registration Details

d018a1b75ae97f09423ac1f97b3e25d6

DHA05603257101

Company Information

Product Details

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

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 16, 2019

Apr 16, 2029