Taiwan FDA registration fea942a3e95ca5e09b52745393b67d29

"Philips" magnetic resonance instrument

TW: “飛利浦”磁共振儀
Taiwan flagTaiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Oct 06, 2008 – Oct 06, 2018Cancelled
Registration details
Analysis ID
fea942a3e95ca5e09b52745393b67d29
Customs Code
DHA00601925607
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
import
Dates and status
Registration Date
Oct 06, 2008
Expiry Date
Oct 06, 2018
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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 fea942a3e95ca5e09b52745393b67d29 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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