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"Singular" ultrasound diagnostic system - Taiwan Registration 746d88cd91e88ba3cfb754da2d91d923

Access comprehensive regulatory information for "Singular" ultrasound diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 746d88cd91e88ba3cfb754da2d91d923 and manufactured by GE HEALTHCARE AUSTRIA GMBH & CO OG. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GE HEALTHCARE AUSTRIA GMBH & CO OG, 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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746d88cd91e88ba3cfb754da2d91d923
Registration Details
Taiwan FDA Registration: 746d88cd91e88ba3cfb754da2d91d923
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Device Details

"Singular" ultrasound diagnostic system
TW: "ๅฅ‡็•ฐ"่ถ…้Ÿณๆณข่จบๆ–ท็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

746d88cd91e88ba3cfb754da2d91d923

DHA00601772700

Company Information

Product Details

For details, please refer to the approved version of Chinese copy

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Jan 26, 2007

Jan 26, 2022

Apr 12, 2024

Cancellation Information

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