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“GE” Ultrasound Probe for medical use - Taiwan Registration 5b0a0c847e2543ea72d4a1c55fcc7d02

Access comprehensive regulatory information for “GE” Ultrasound Probe for medical use in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5b0a0c847e2543ea72d4a1c55fcc7d02 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, 2 companies making similar products including GE Parallel Design, Inc., GE VINGMED ULTRASOUND AS, and 2 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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5b0a0c847e2543ea72d4a1c55fcc7d02
Registration Details
Taiwan FDA Registration: 5b0a0c847e2543ea72d4a1c55fcc7d02
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Device Details

“GE” Ultrasound Probe for medical use
TW: “奇異”診斷用超音波探頭
Risk Class 2
MD

Registration Details

5b0a0c847e2543ea72d4a1c55fcc7d02

Ministry of Health Medical Device Import No. 030438

DHA05603043802

Company Information

Product Details

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

P Devices for radiology

P1570 Ultrasound converter for diagnostics

Imported from abroad

Dates and Status

Nov 22, 2017

Nov 22, 2027

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