Taiwan FDA registration 23726cd3794cb1d7209ac134c82484fa

"Singular" positron/computed tomography system

TW: “奇異”正子/電腦斷層掃描系統
Taiwan flagTaiwan·Risk Class 2·GE MEDICAL SYSTEMS·Registered Dec 19, 2011 – Dec 19, 2026Active
Registration details
Analysis ID
23726cd3794cb1d7209ac134c82484fa
Customs Code
DHAS0602311104
Company information
Manufacturer
GE MEDICAL SYSTEMS
Manufacturer Country
United States
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.1200 Radiology CT system
Import Information
Input;; The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". 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
Dec 19, 2011
Expiry Date
Dec 19, 2026
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About this record

Access comprehensive regulatory information for "Singular" positron/computed tomography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 23726cd3794cb1d7209ac134c82484fa and manufactured by GE MEDICAL SYSTEMS. 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 GE MEDICAL SYSTEMS, GE MEDICAL SYSTEMS, LLC, 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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