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"Tonoki" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration 322143b3a94248047b8eb468750df14a

Access comprehensive regulatory information for "Tonoki" 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 322143b3a94248047b8eb468750df14a and manufactured by TOSHIBA ELECTRON TUBES & DEVICES CO., LTD.. The authorized representative in Taiwan is WITTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TOSHIBA ELECTRON TUBES & DEVICES CO., LTD., and 1 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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322143b3a94248047b8eb468750df14a
Registration Details
Taiwan FDA Registration: 322143b3a94248047b8eb468750df14a
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Device Details

"Tonoki" diagnostic X-ray tube sleeve assembly (unsterilized)
TW: "ๆฑไน‹"่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

322143b3a94248047b8eb468750df14a

DHAS4401186800

Company Information

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

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Jun 25, 2012

Jun 25, 2022

Apr 12, 2024

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ

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