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“Philips” Affiniti Series Ultrasound System - Taiwan Registration cac5a9fa998e4de0e42fc141f0b7d4c2

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 cac5a9fa998e4de0e42fc141f0b7d4c2 and manufactured by 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 For use only by the Parts System Denda;;For spare parts system only;;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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Registration Details
Taiwan FDA Registration: cac5a9fa998e4de0e42fc141f0b7d4c2
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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

cac5a9fa998e4de0e42fc141f0b7d4c2

Ministry of Health Medical Device Import No. 034861

DHA05603486104

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

P Devices for radiology

P1550 ultrasonic pulsating Doppler imaging system

Imported from abroad

Dates and Status

Sep 14, 2021

Sep 14, 2026

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