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"Singular" ultrasound diagnostic system - Taiwan Registration 862893960e0e4cdc4ed48d3c593ecf4b

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 862893960e0e4cdc4ed48d3c593ecf4b 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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862893960e0e4cdc4ed48d3c593ecf4b
Registration Details
Taiwan FDA Registration: 862893960e0e4cdc4ed48d3c593ecf4b
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Device Details

"Singular" ultrasound diagnostic system
TW: โ€œๅฅ‡็•ฐโ€่ถ…้Ÿณๆณข่จบๆ–ท็ณป็ตฑ
Risk Class 2

Registration Details

862893960e0e4cdc4ed48d3c593ecf4b

DHA00601802802

Company Information

Product Details

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

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Apr 19, 2007

Apr 19, 2027

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