Taiwan FDA registration 5b0a0c847e2543ea72d4a1c55fcc7d02

“GE” Ultrasound Probe for medical use

TW: “奇異”診斷用超音波探頭
Taiwan flagTaiwan·Risk Class 2·MD·GE HEALTHCARE AUSTRIA GMBH & CO OG·Registered Nov 22, 2017 – Nov 22, 2027Active
Registration details
Analysis ID
5b0a0c847e2543ea72d4a1c55fcc7d02
License Form
Ministry of Health Medical Device Import No. 030438
Customs Code
DHA05603043802
Company information
Manufacturer Country
Austria
Authorized Representative
GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Devices for radiology
Product Type (Level 2)
P1570 Ultrasound converter for diagnostics
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 22, 2017
Expiry Date
Nov 22, 2027
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About this record

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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