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"Philips" computed tomography diagnostic device - Taiwan Registration 45d8b3a90e896b331fe60e551df85e21

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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45d8b3a90e896b331fe60e551df85e21
Registration Details
Taiwan FDA Registration: 45d8b3a90e896b331fe60e551df85e21
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Device Details

"Philips" computed tomography diagnostic device
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ ้›ป่…ฆๆ–ทๅฑคๆ”ๅฝฑ่จบๆ–ท่ฃ็ฝฎ
Risk Class 2
Cancelled

Registration Details

45d8b3a90e896b331fe60e551df85e21

DHAS5602602302

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1750 ้›ป่…ฆๆ–ทๅฑคๆŽƒๆXๅ…‰็ณป็ตฑ

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

Mar 25, 2014

Mar 25, 2019

Jul 15, 2022

Cancellation Information

Logged out

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