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"Philips" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration ea4af38da170685dc1f1f0cc1c170700

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 ea4af38da170685dc1f1f0cc1c170700 and manufactured by GILARDONI S.P.A.. 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, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., 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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ea4af38da170685dc1f1f0cc1c170700
Registration Details
Taiwan FDA Registration: ea4af38da170685dc1f1f0cc1c170700
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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

Registration Details

ea4af38da170685dc1f1f0cc1c170700

DHAS9402020501

Company Information

Italy

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

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 19, 2019

Mar 19, 2029