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“Philips” 5000 Compact Series Ultrasound Systems - Taiwan Registration 6962109ea7675e035caae436b7323f18

Access comprehensive regulatory information for “Philips” 5000 Compact Series 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 6962109ea7675e035caae436b7323f18 and manufactured by 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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6962109ea7675e035caae436b7323f18
Registration Details
Taiwan FDA Registration: 6962109ea7675e035caae436b7323f18
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Device Details

“Philips” 5000 Compact Series Ultrasound Systems
TW: “飛利浦” 超音波系統
Risk Class 2
MD

Registration Details

6962109ea7675e035caae436b7323f18

Ministry of Health Medical Device Import No. 036577

DHA05603657704

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

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Imported from abroad

Dates and Status

Aug 13, 2023

Aug 13, 2028