Taiwan FDA registration 894858bf649fcce3d88b391e61038420

"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 Mar 02, 2018 – Mar 02, 2028Active
Registration details
Analysis ID
894858bf649fcce3d88b391e61038420
Customs Code
DHA05603075001
Company information
Manufacturer Country
Netherlands
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1000 磁振診斷裝置
Import Information
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
Registration Date
Mar 02, 2018
Expiry Date
Mar 02, 2028
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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 894858bf649fcce3d88b391e61038420 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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