Taiwan FDA registration 9ba5c2cace09966e5e01966402b281af

"Philips" magnetic resonance imaging system

TW: “飛利浦” 磁振造影系統
Taiwan flagTaiwan·Risk Class 2·Philips Medical Systems Nederland B.V.·Registered Jul 28, 2021 – Jul 28, 2026Expired
Registration details
Analysis ID
9ba5c2cace09966e5e01966402b281af
Customs Code
DHA05603477307
Company information
Manufacturer Country
Netherlands
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1000 磁振診斷裝置
Import Information
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
Registration Date
Jul 28, 2021
Expiry Date
Jul 28, 2026
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About this record

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 9ba5c2cace09966e5e01966402b281af 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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