Taiwan FDA registration 862893960e0e4cdc4ed48d3c593ecf4b

"Singular" ultrasound diagnostic system

TW: “奇異”超音波診斷系統
Taiwan flagTaiwan·Risk Class 2·GE HEALTHCARE AUSTRIA GMBH & CO OG·Registered Apr 19, 2007 – Apr 19, 2027Active
Registration details
Analysis ID
862893960e0e4cdc4ed48d3c593ecf4b
Customs Code
DHA00601802802
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 Radiology Science
Product Type (Level 2)
P.1550 Ultrasonic pulsating Duppler imaging system
Import Information
import
Dates and status
Registration Date
Apr 19, 2007
Expiry Date
Apr 19, 2027
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About this record

Access comprehensive regulatory information for "Singular" ultrasound diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 862893960e0e4cdc4ed48d3c593ecf4b 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, 1 companies making similar products including GE HEALTHCARE AUSTRIA GMBH & CO OG, and 1 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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