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“Philips” Quantification Software - Taiwan Registration ea383c231ee8240e2f855136be691acb

Access comprehensive regulatory information for “Philips” Quantification Software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea383c231ee8240e2f855136be691acb and manufactured by Philips Ultrasound, LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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ea383c231ee8240e2f855136be691acb
Registration Details
Taiwan FDA Registration: ea383c231ee8240e2f855136be691acb
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Device Details

“Philips” Quantification Software
TW: “飛利浦” 定量軟體
Risk Class 2
MD

Registration Details

ea383c231ee8240e2f855136be691acb

Ministry of Health Medical Device Import No. 026591

DHA05602659105

Company Information

United States

Product Details

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

P Devices for radiology

P2050 Medical Image Management and Processing System

Imported from abroad

Dates and Status

Oct 21, 2014

Oct 21, 2024