Taiwan FDA registration eed831a2a6c12f69a4d373cd9e375112

"Bizarre" angiogram X-ray system

TW: “奇異”血管攝影X光系統
Taiwan flagTaiwan·Risk Class 2·GE MEDICAL SYSTEMS S.C.S·Registered Jan 31, 2013 – Jan 31, 2028Active
Registration details
Analysis ID
eed831a2a6c12f69a4d373cd9e375112
Customs Code
DHAS0602440704
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
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
Registration Date
Jan 31, 2013
Expiry Date
Jan 31, 2028
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About this record

Access comprehensive regulatory information for "Bizarre" angiogram 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 eed831a2a6c12f69a4d373cd9e375112 and manufactured by GE MEDICAL SYSTEMS S.C.S. 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 MEDICAL SYSTEMS S.A., GE HUALUN MEDICAL SYSTEMS CO., LTD., 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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