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“Philips” IntelliVue Patient Monitor - Taiwan Registration d5bc5ce47ecf94dd650ff9188d0ae007

Access comprehensive regulatory information for “Philips” IntelliVue Patient Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d5bc5ce47ecf94dd650ff9188d0ae007 and manufactured by For use only by the Parts System Denda;;For spare parts system only;;Philips Medizin Systeme Böblingen 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 MEDIZINSYSTEME BÖBLINGEN GMBH, and 1 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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d5bc5ce47ecf94dd650ff9188d0ae007
Registration Details
Taiwan FDA Registration: d5bc5ce47ecf94dd650ff9188d0ae007
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Device Details

“Philips” IntelliVue Patient Monitor
TW: “飛利浦” 病患監視器
Risk Class 2
MD

Registration Details

d5bc5ce47ecf94dd650ff9188d0ae007

Ministry of Health Medical Device Import No. 034602

DHA05603460206

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E1025 Arrhythmia detector and alert

Imported from abroad

Dates and Status

Oct 19, 2021

Oct 19, 2026

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