Taiwan FDA registration 45d8b3a90e896b331fe60e551df85e21

"Philips" computed tomography diagnostic device

TW: “飛利浦” 電腦斷層攝影診斷裝置
Taiwan flagTaiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.·Registered Mar 25, 2014 – Mar 25, 2019Cancelled
Registration details
Analysis ID
45d8b3a90e896b331fe60e551df85e21
Customs Code
DHAS5602602302
Company information
Manufacturer Country
United States
Authorized Representative
PHILIPS TAIWAN LIMITED
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
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;; 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
Mar 25, 2014
Expiry Date
Mar 25, 2019
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Philips" computed tomography diagnostic device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 45d8b3a90e896b331fe60e551df85e21 and manufactured by PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including Philips Healthcare (Suzhou) Co., Ltd, PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC., 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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