Taiwan FDA registration 4e186a45af33c24f65cf9ec9b7545e6f

"Fujifilm Film" whole body computed tomography X-ray device

TW: “富士軟片”全身電腦斷層X光線裝置
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa·Registered Jun 15, 2020 – Jun 15, 2025Expired
Registration details
Analysis ID
4e186a45af33c24f65cf9ec9b7545e6f
Customs Code
DHAS5603376409
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., 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.1750 電腦斷層掃描X光系統
Import Information
Input;; 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.
Dates and status
Registration Date
Jun 15, 2020
Expiry Date
Jun 15, 2025
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About this record

Access comprehensive regulatory information for "Fujifilm Film" whole body computed tomography X-ray device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4e186a45af33c24f65cf9ec9b7545e6f and manufactured by FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa, and 1 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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