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"Philips" computed tomography diagnostic device - Taiwan Registration 23addef40caa63d22099d7c5b1c6baab

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 23addef40caa63d22099d7c5b1c6baab and manufactured by Philips Healthcare (Suzhou) Co., Ltd. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC., PHILIPS MEDICAL SYSTEM TECHNOLOGIES LTD., 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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23addef40caa63d22099d7c5b1c6baab
Registration Details
Taiwan FDA Registration: 23addef40caa63d22099d7c5b1c6baab
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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

23addef40caa63d22099d7c5b1c6baab

DHAS9200063903

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

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

Dec 11, 2014

Mar 25, 2024

Sep 10, 2020

Cancellation Information

Logged out

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