Taiwan FDA registration f01beb51ed9ef69f2b1e68d40b2d8be6

"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, LLC·Registered Aug 25, 2009 – Aug 25, 2029Active
Registration details
Analysis ID
f01beb51ed9ef69f2b1e68d40b2d8be6
Customs Code
DHAS0602014101
Company information
Manufacturer Country
United States
Authorized Representative
GE MEDICAL SYSTEMS TAIWAN, LTD.
Product details
Intended Use
For details Chinese imitation of the single He Definitive Version
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1750 Computed tomography X-ray system;; P.1200 Radiology CT system
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); 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". input
Dates and status
Registration Date
Aug 25, 2009
Expiry Date
Aug 25, 2029
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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 f01beb51ed9ef69f2b1e68d40b2d8be6 and manufactured by GE MEDICAL SYSTEMS, LLC. 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 ISRAEL-FUNCTIONAL IMAGING, 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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