Taiwan FDA registration c457ce1b56acd2ae60ca9b82e74b115c

“GE” Ultrasound Probe for medical use

TW: “奇異”診斷用超音波探頭
Taiwan flagTaiwan·Risk Class 2·MD·GE Parallel Design, Inc.·Registered Nov 20, 2017 – Nov 20, 2027Active
Registration details
Analysis ID
c457ce1b56acd2ae60ca9b82e74b115c
License Form
Ministry of Health Medical Device Import No. 030429
Customs Code
DHA05603042901
Company information
Manufacturer Country
United States
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 20, 2017
Expiry Date
Nov 20, 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 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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