Taiwan FDA registration ccf608af9446d4d9aa6db947a42c70c3

"Singular" X-ray system

TW: “奇異”X光系統
Taiwan flagTaiwan·Risk Class 2·GE MEDICAL SYSTEMS S.A.·Registered Dec 18, 2012 – Dec 18, 2027Active
Registration details
Analysis ID
ccf608af9446d4d9aa6db947a42c70c3
Customs Code
DHAS0602426102
Company information
Manufacturer Country
France
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.1600 X光血管攝影系統
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
Registration Date
Dec 18, 2012
Expiry Date
Dec 18, 2027
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About this record

Access comprehensive regulatory information for "Singular" X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ccf608af9446d4d9aa6db947a42c70c3 and manufactured by GE MEDICAL SYSTEMS S.A.. 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 NRT-NORDISK X-RAY TECHNIQUE A/S, 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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