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"Dunley" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration 745c9319fe5c5e0ffc9876dbddd49a5c

Access comprehensive regulatory information for "Dunley" 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 745c9319fe5c5e0ffc9876dbddd49a5c and manufactured by DUNLEE. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

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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745c9319fe5c5e0ffc9876dbddd49a5c
Registration Details
Taiwan FDA Registration: 745c9319fe5c5e0ffc9876dbddd49a5c
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Device Details

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

Registration Details

745c9319fe5c5e0ffc9876dbddd49a5c

DHAS4400607408

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

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

Dates and Status

Aug 08, 2007

Aug 08, 2012

Apr 30, 2014

Cancellation Information

Logged out

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