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"Philips" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration 895292ddfbd328bdf2332131186a08b1

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 895292ddfbd328bdf2332131186a08b1 and manufactured by SPELLMAN DE MEXICO, S.A. DE C.V. PLANTA 3. 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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895292ddfbd328bdf2332131186a08b1
Registration Details
Taiwan FDA Registration: 895292ddfbd328bdf2332131186a08b1
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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

Registration Details

895292ddfbd328bdf2332131186a08b1

DHAS9402018202

Company Information

Product Details

Limited to the first level identification range of the "X-ray tube sleeve assembly for diagnosis (P.1760)" of the Measures for the Classification and Grading Management of Medical Equipment.

P Radiology Science

P.1760 ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ

Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Mar 13, 2019

Mar 13, 2024