“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.
Device Details
Registration Details
d5bc5ce47ecf94dd650ff9188d0ae007
Ministry of Health Medical Device Import No. 034602
DHA05603460206
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

