Taiwan FDA registration 746d88cd91e88ba3cfb754da2d91d923

"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 Jan 26, 2007 – Jan 26, 2022Cancelled
Registration details
Analysis ID
746d88cd91e88ba3cfb754da2d91d923
Customs Code
DHA00601772700
Company information
Manufacturer Country
Austria
Authorized Representative
GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
Intended Use
For details, please refer to the approved version of Chinese copy
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
Jan 26, 2007
Expiry Date
Jan 26, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 746d88cd91e88ba3cfb754da2d91d923 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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