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“Philips” IntelliVue Information Center iX - Taiwan Registration d460cec149fa543eabd4f61333a688a3

Access comprehensive regulatory information for “Philips” IntelliVue Information Center iX in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d460cec149fa543eabd4f61333a688a3 and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including PHILIPS MEDICAL SYSTEMS, PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH, and 2 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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d460cec149fa543eabd4f61333a688a3
Registration Details
Taiwan FDA Registration: d460cec149fa543eabd4f61333a688a3
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Device Details

“Philips” IntelliVue Information Center iX
TW: “飛利浦”中央監視站軟體
Risk Class 2
MD
Cancelled

Registration Details

d460cec149fa543eabd4f61333a688a3

Ministry of Health Medical Device Import No. 027262

DHA05602726204

Company Information

United States

Product Details

E Cardiovascular devices

E1025 Arrhythmia detector and alert

Imported from abroad

Dates and Status

Apr 16, 2015

Apr 16, 2020

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者

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