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“GE” Ultrasound Probe for medical use - Taiwan Registration c457ce1b56acd2ae60ca9b82e74b115c

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 c457ce1b56acd2ae60ca9b82e74b115c and manufactured by GE Parallel Design, Inc.. 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 HEALTHCARE AUSTRIA GMBH & CO OG, 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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c457ce1b56acd2ae60ca9b82e74b115c
Registration Details
Taiwan FDA Registration: c457ce1b56acd2ae60ca9b82e74b115c
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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

c457ce1b56acd2ae60ca9b82e74b115c

Ministry of Health Medical Device Import No. 030429

DHA05603042901

Company Information

United States

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 20, 2017

Nov 20, 2027

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