Philips IntelliVue MP2 Patient Monitor - HSA Registration DE0015026
Access comprehensive regulatory information for Philips IntelliVue MP2 Patient Monitor in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0015026 and owned by Philips Medizin Systeme Böblingen GmbH. The device was registered on March 27, 2014.
This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
For monitoring/recording/generating alarms for multiple physiological parameters of adults, pediatrics and neonates in hospital environments and transporting patients inside/outside hospital. It is only for use on one patient at a time and not intended for home use. It is not a therapeutic device. ST segment monitoring is intended for use with adult patients only and is not clinically validated for use with neonatal and pediatric patients. The ECG measurement is intended to be used for diagnostic recording of rhythm and detailed morphology of complex cardiac complexes. The Integrated Pulmonary Index is intended for use with adult and pediatric (1 -12 years) patients only. The IPI is an adjunct to and not intended to replace vital sign monitoring. The derived measurement Pulse Pressure Variation is intended for use with sedated patients receiving controlled mechanical ventilation and mainly free from cardiac arrhythmia. The PPV measurement has been validated only for adult patients.