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"Philips" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration cf7e1ffbcd0e6df5b5d9e34c378e66dd

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 cf7e1ffbcd0e6df5b5d9e34c378e66dd and manufactured by PHILIPS MEDICAL SYSTEMS DMC GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 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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cf7e1ffbcd0e6df5b5d9e34c378e66dd
Registration Details
Taiwan FDA Registration: cf7e1ffbcd0e6df5b5d9e34c378e66dd
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Device Details

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

Registration Details

cf7e1ffbcd0e6df5b5d9e34c378e66dd

DHAS4401313009

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

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Jun 21, 2013

Jun 21, 2018

Dec 13, 2019

Cancellation Information

Logged out

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