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"Philips" X-ray system - Taiwan Registration f05f32571436ea1520de47d84419bc31

Access comprehensive regulatory information for "Philips" 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 f05f32571436ea1520de47d84419bc31 and manufactured by PHILIPS MEDICAL SYSTEMS DMC GMBH;; PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Philips Medical Systems Nederland B.V., PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., and 5 recent registrations in the same category. 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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f05f32571436ea1520de47d84419bc31
Registration Details
Taiwan FDA Registration: f05f32571436ea1520de47d84419bc31
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Device Details

"Philips" X-ray system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€Xๅ…‰็ณป็ตฑ
Risk Class 2

Registration Details

f05f32571436ea1520de47d84419bc31

DHAS5603025502

Company Information

Product Details

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

P Radiology Science

P.1650 ้€่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

Sep 20, 2017

Sep 20, 2027