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"Qi Yi Mead" X-ray tube sleeve assembly for diagnosis (unsterilized) - Taiwan Registration 4e45f53aa0002030172d139ceae09328

Access comprehensive regulatory information for "Qi Yi Mead" X-ray tube sleeve assembly for diagnosis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4e45f53aa0002030172d139ceae09328 and manufactured by GE MEDICAL SYSTEMS S.A.. The authorized representative in Taiwan is DR. MEDICOM CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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4e45f53aa0002030172d139ceae09328
Registration Details
Taiwan FDA Registration: 4e45f53aa0002030172d139ceae09328
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Device Details

"Qi Yi Mead" X-ray tube sleeve assembly for diagnosis (unsterilized)
TW: "้ฝŠ็ฟŒ็พŽๅพท" ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

4e45f53aa0002030172d139ceae09328

DHAS9402173901

Company Information

France

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

Jul 14, 2020

Jul 14, 2025