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"Philips" Diagnostic x-ray tube housing assembly (Non-Sterile) - Taiwan Registration a743210b11b806e30218082b50f1eb42

Access comprehensive regulatory information for "Philips" Diagnostic x-ray tube housing assembly (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a743210b11b806e30218082b50f1eb42 and manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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a743210b11b806e30218082b50f1eb42
Registration Details
Taiwan FDA Registration: a743210b11b806e30218082b50f1eb42
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Device Details

"Philips" Diagnostic x-ray tube housing assembly (Non-Sterile)
TW: "้ฃ›ๅˆฉๆตฆ" ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a743210b11b806e30218082b50f1eb42

Ministry of Health Medical Device Import No. 016764

DHAS9401676406

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 Devices for radiology

P1760 X-ray tube sleeve assembly for diagnostics

Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)

Dates and Status

Jul 11, 2016

Jul 11, 2026