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X-ray tube sleeve assembly for diagnostic "lightning" (unsterilized) - Taiwan Registration cb26604a1bbfe5fce63801aa706d661c

Access comprehensive regulatory information for X-ray tube sleeve assembly for diagnostic "lightning" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cb26604a1bbfe5fce63801aa706d661c and manufactured by SOURCE-RAY, INC.. The authorized representative in Taiwan is Taiwan Tengxie Biotechnology 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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cb26604a1bbfe5fce63801aa706d661c
Registration Details
Taiwan FDA Registration: cb26604a1bbfe5fce63801aa706d661c
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Device Details

X-ray tube sleeve assembly for diagnostic "lightning" (unsterilized)
TW: "ๅฎˆ้›ท"่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

cb26604a1bbfe5fce63801aa706d661c

DHAS4401080204

Company Information

United States

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

Sep 05, 2011

Sep 05, 2016

Aug 14, 2018

Cancellation Information

Logged out

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