Taiwan FDA registration b4ff01217c5a4a400ea3133579d679a9

"Singular" diagnostic X-ray machine

TW: "奇異" 診斷型X光機
Taiwan flagTaiwan·Risk Class 2·GE HUALUN MEDICAL SYSTEMS CO., LTD.·Registered Jun 10, 2005 – Jun 10, 2020Cancelled
Registration details
Analysis ID
b4ff01217c5a4a400ea3133579d679a9
Customs Code
DHAS4200001906
Company information
Manufacturer Country
China
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.1680 固定式X光系統
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); Chinese goods;; input
Dates and status
Registration Date
Jun 10, 2005
Expiry Date
Jun 10, 2020
Cancellation Date
Jun 22, 2022
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" diagnostic X-ray machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b4ff01217c5a4a400ea3133579d679a9 and manufactured by GE HUALUN MEDICAL SYSTEMS CO., LTD.. 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 HUALUN MEDICAL SYSTEMS CO., LTD., and 3 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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