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X-ray tube sleeve assembly for diagnostic "ENDI" (unsterilized) - Taiwan Registration 887683155dcc8d58dbbcdb47464920ac

Access comprehensive regulatory information for X-ray tube sleeve assembly for diagnostic "ENDI" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 887683155dcc8d58dbbcdb47464920ac and manufactured by IMD GENERATORS SRL. The authorized representative in Taiwan is INNOMED INTERNATIONAL INC..

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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887683155dcc8d58dbbcdb47464920ac
Registration Details
Taiwan FDA Registration: 887683155dcc8d58dbbcdb47464920ac
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Device Details

X-ray tube sleeve assembly for diagnostic "ENDI" (unsterilized)
TW: โ€œ่‰พๆฉ่ฟชโ€่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

887683155dcc8d58dbbcdb47464920ac

DHAS4401129505

Company Information

Italy

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "X-ray Tube Sleeve Components for Diagnosis (P.1760)".

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 13, 2012

Jan 13, 2022

Apr 12, 2024

Cancellation Information

Logged out

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