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“Philips” IntelliVue Patient Monitor - Taiwan Registration 02fc972bcda9de9d474df85de845db26

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 02fc972bcda9de9d474df85de845db26 and manufactured by PHILIPS MEDIZINSYSTEME 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 For use only by the Parts System Denda;;For spare parts system only;;Philips Medizin Systeme 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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02fc972bcda9de9d474df85de845db26
Registration Details
Taiwan FDA Registration: 02fc972bcda9de9d474df85de845db26
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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

02fc972bcda9de9d474df85de845db26

Ministry of Health Medical Device Import No. 026679

DHA05602667906

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

Nov 19, 2014

Nov 19, 2024

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