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“Philips” EPIQ Series Diagnostic Ultrasound Systems - Taiwan Registration 7d901a9d7774e2522d6511397a42438d

Access comprehensive regulatory information for “Philips” EPIQ Series Diagnostic Ultrasound Systems in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d901a9d7774e2522d6511397a42438d and manufactured by For use only by the Parts System Denda;;For spare parts system only;;Philips Ultrasound, LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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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7d901a9d7774e2522d6511397a42438d
Registration Details
Taiwan FDA Registration: 7d901a9d7774e2522d6511397a42438d
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Device Details

“Philips” EPIQ Series Diagnostic Ultrasound Systems
TW: “飛利浦” 超音波系統
Risk Class 2
MD

Registration Details

7d901a9d7774e2522d6511397a42438d

Ministry of Health Medical Device Import No. 034753

DHA05603475301

Company Information

Product Details

Details are as detailed as approved Chinese instructions

P Devices for radiology

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Imported from abroad

Dates and Status

Jul 07, 2021

Jul 07, 2026