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“Philips” Affiniti Series Ultrasound System - Taiwan Registration e7ecf51a1baee61175c3def62d12d24e

Access comprehensive regulatory information for “Philips” Affiniti Series Ultrasound System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e7ecf51a1baee61175c3def62d12d24e 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, 1 companies making similar products including Philips Ultrasound, LLC, 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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e7ecf51a1baee61175c3def62d12d24e
Registration Details
Taiwan FDA Registration: e7ecf51a1baee61175c3def62d12d24e
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Device Details

“Philips” Affiniti Series Ultrasound System
TW: “飛利浦”超音波系統
Risk Class 2
MD

Registration Details

e7ecf51a1baee61175c3def62d12d24e

Ministry of Health Medical Device Import No. 027013

DHA05602701309

Company Information

Product Details

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

P Devices for radiology

P1550 ultrasonic pulsating Doppler imaging system

Imported from abroad

Dates and Status

Feb 10, 2015

Feb 10, 2025

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