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“GE” Ultrasound Probe for medical use - Taiwan Registration b360d5c54bc94c907d8e94e5458347ad

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 b360d5c54bc94c907d8e94e5458347ad and manufactured by GE VINGMED ULTRASOUND AS. 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 HEALTHCARE AUSTRIA GMBH & CO OG, 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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b360d5c54bc94c907d8e94e5458347ad
Registration Details
Taiwan FDA Registration: b360d5c54bc94c907d8e94e5458347ad
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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

b360d5c54bc94c907d8e94e5458347ad

Ministry of Health Medical Device Import No. 030183

DHA05603018305

Company Information

Norway

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

Sep 08, 2017

Sep 08, 2027

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