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"Philips" fluoroscopic X-ray system - Taiwan Registration ed5434f4e5800cae1eb8c9fdd8936bf3

Access comprehensive regulatory information for "Philips" fluoroscopic 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 ed5434f4e5800cae1eb8c9fdd8936bf3 and manufactured by PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.. 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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ed5434f4e5800cae1eb8c9fdd8936bf3
Registration Details
Taiwan FDA Registration: ed5434f4e5800cae1eb8c9fdd8936bf3
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Device Details

"Philips" fluoroscopic X-ray system
TW: "้ฃ›ๅˆฉๆตฆ"้€่ฆ–Xๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

ed5434f4e5800cae1eb8c9fdd8936bf3

DHAS4200014409

Company Information

Product Details

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

P Radiology Science

P.1660 ้ž้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

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

Nov 03, 2006

Nov 03, 2016

Apr 25, 2018

Cancellation Information

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