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"Bizarre" angiogram X-ray system - Taiwan Registration eed831a2a6c12f69a4d373cd9e375112

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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eed831a2a6c12f69a4d373cd9e375112
Registration Details
Taiwan FDA Registration: eed831a2a6c12f69a4d373cd9e375112
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Device Details

"Bizarre" angiogram X-ray system
TW: โ€œๅฅ‡็•ฐโ€่ก€็ฎกๆ”ๅฝฑXๅ…‰็ณป็ตฑ
Risk Class 2

Registration Details

eed831a2a6c12f69a4d373cd9e375112

DHAS0602440704

Company Information

France

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1600 Xๅ…‰่ก€็ฎกๆ”ๅฝฑ็ณป็ตฑ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Jan 31, 2013

Jan 31, 2028

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