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"Philips" multifunctional digital X-ray system - Taiwan Registration 10610b1fd4075c9dab931792fa46559a

Access comprehensive regulatory information for "Philips" multifunctional digital X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 10610b1fd4075c9dab931792fa46559a and manufactured by PHILIPS MEDICAL SYSTEMS DMC GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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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10610b1fd4075c9dab931792fa46559a
Registration Details
Taiwan FDA Registration: 10610b1fd4075c9dab931792fa46559a
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Device Details

"Philips" multifunctional digital X-ray system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ๅคšๅŠŸ่ƒฝๆ•ธไฝXๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

10610b1fd4075c9dab931792fa46559a

DHAS0601816405

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

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

Dates and Status

Jul 16, 2007

Jul 16, 2017

Dec 13, 2019

Cancellation Information

Logged out

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