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"Singular" fluoroscopic X-ray system - Taiwan Registration c3ab9d1a15a661c21c0fc6a91c476608

Access comprehensive regulatory information for "Singular" fluoroscopic 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 c3ab9d1a15a661c21c0fc6a91c476608 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, 3 companies making similar products including GENERAL MEDICAL MERATE S.P.A., GE MEDICAL SYSTEMS S.A., and 5 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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c3ab9d1a15a661c21c0fc6a91c476608
Registration Details
Taiwan FDA Registration: c3ab9d1a15a661c21c0fc6a91c476608
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Device Details

"Singular" fluoroscopic X-ray system
TW: "ๅฅ‡็•ฐ"้€่ฆ–Xๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

c3ab9d1a15a661c21c0fc6a91c476608

DHAS0601710701

Company Information

France

Product Details

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

P Radiology Science

P.1650 ้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

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

Sep 12, 2006

Sep 12, 2016

Apr 25, 2018

Cancellation Information

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