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X-ray tube sleeve assembly for diagnostic "Dengli" (unsterilized) - Taiwan Registration a2832fd4b706924b74e30707b42aed38

Access comprehensive regulatory information for X-ray tube sleeve assembly for diagnostic "Dengli" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a2832fd4b706924b74e30707b42aed38 and manufactured by DUNLEE. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DUNLEE, and 2 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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a2832fd4b706924b74e30707b42aed38
Registration Details
Taiwan FDA Registration: a2832fd4b706924b74e30707b42aed38
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Device Details

X-ray tube sleeve assembly for diagnostic "Dengli" (unsterilized)
TW: โ€œ็™ป็ซ‹โ€่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

a2832fd4b706924b74e30707b42aed38

DHAS4400978708

Company Information

United States

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

Jan 10, 2011

Jan 10, 2026

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