Taiwan FDA registration 26fd8c5897b906a8820e054ab19eb509

"Philips" magnetic resonance instrument

TW: "飛利浦" 磁共振儀
Taiwan flagTaiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Dec 26, 2003 – Dec 26, 2028Active
Registration details
Analysis ID
26fd8c5897b906a8820e054ab19eb509
Customs Code
DHA00601049200
Company information
Manufacturer Country
Netherlands
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Product Type (Level 1)
P Radiology Science
Import Information
import
Dates and status
Registration Date
Dec 26, 2003
Expiry Date
Dec 26, 2028
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About this record

Access comprehensive regulatory information for "Philips" magnetic resonance instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 26fd8c5897b906a8820e054ab19eb509 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, 1 companies making similar products including PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., and 1 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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