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“Philips” IntelliVue Information Center iX - Taiwan Registration 377ce9ab0e5fa6cfa816d5bfd7c917de

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 377ce9ab0e5fa6cfa816d5bfd7c917de and manufactured by PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHILIPS MEDICAL SYSTEMS, 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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377ce9ab0e5fa6cfa816d5bfd7c917de
Registration Details
Taiwan FDA Registration: 377ce9ab0e5fa6cfa816d5bfd7c917de
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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

Registration Details

377ce9ab0e5fa6cfa816d5bfd7c917de

Ministry of Health Medical Device Import No. 033071

DHA05603307109

Company Information

Product Details

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

E Cardiovascular devices

E1025 Arrhythmia detector and alert

Imported from abroad

Dates and Status

Dec 19, 2019

Dec 19, 2024

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