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"Dangli" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration 1f25682bd1eae6ad91fc8da3b0a3f446

Access comprehensive regulatory information for "Dangli" 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 1f25682bd1eae6ad91fc8da3b0a3f446 and manufactured by DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC. The authorized representative in Taiwan is UNISON COMPANY LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including DUNLEE, DUNLEE, A DIVISION OF PHILIPS MEDICAL SYSTEMS, CLEVELAND, INC, and 3 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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1f25682bd1eae6ad91fc8da3b0a3f446
Registration Details
Taiwan FDA Registration: 1f25682bd1eae6ad91fc8da3b0a3f446
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Device Details

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

Registration Details

1f25682bd1eae6ad91fc8da3b0a3f446

DHAS9401419700

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

May 30, 2014

May 30, 2024