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"Philips" magnetic resonance imaging system - Taiwan Registration 3d8e1707a0eb430cba8e9a6ae1ed6764

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 3d8e1707a0eb430cba8e9a6ae1ed6764 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 Healthcare (Suzhou) Co., Ltd, 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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3d8e1707a0eb430cba8e9a6ae1ed6764
Registration Details
Taiwan FDA Registration: 3d8e1707a0eb430cba8e9a6ae1ed6764
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Device Details

"Philips" magnetic resonance imaging system
TW: "้ฃ›ๅˆฉๆตฆ" ็ฃๆŒฏ้€ ๅฝฑ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

3d8e1707a0eb430cba8e9a6ae1ed6764

DHA00601386604

Company Information

Product Details

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

P Radiology Science

import

Dates and Status

Jan 09, 2006

Jan 09, 2021

Sep 08, 2023

Cancellation Information

Logged out

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