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"Philips" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration 14cf4260af3071903d7bb01749538d8f

Access comprehensive regulatory information for "Philips" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 14cf4260af3071903d7bb01749538d8f and manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including PHILIPS MEDICAL SYSTEMS DMC GMBH, GILARDONI S.P.A., 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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14cf4260af3071903d7bb01749538d8f
Registration Details
Taiwan FDA Registration: 14cf4260af3071903d7bb01749538d8f
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Device Details

"Philips" diagnostic X-ray tube sleeve assembly (unsterilized)
TW: "้ฃ›ๅˆฉๆตฆ" ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

14cf4260af3071903d7bb01749538d8f

DHA04401055900

Company Information

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "X-ray Tube Sleeve Components for Diagnosis (P.1760)".

P Radiology Science

P.1760 ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ

import

Dates and Status

Jul 08, 2011

Jul 08, 2016

Apr 25, 2018

Cancellation Information

Logged out

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