Philips IntelliVue Multi-Measurement Module and Patient Monitor - HSA Registration DE0015024
Access comprehensive regulatory information for Philips IntelliVue Multi-Measurement Module and 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 DE0015024 and owned by Philips Medizin Systeme Bรถblingen 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.
The monitor is intended to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates. ECG measurement is intended for diagnostic recording of rhythm and detailed morphology of complex cardiac complexes. Integrated Pulmonary Index is intended for use with adult and pediatric (1 to 12 years) patients only. Pulse Pressure Variation (PPV) is intended for use with sedated patients receiving controlled mechanical ventilation and mainly free from cardiac arrhythmia. The PPV measurement and ST segment monitoring are intended for use with adult patients only. The Masimo rainbow SET measurement is indicated for the noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2), pulse rate, carboxyhemoglobin saturation (SpCO), methemoglobin saturation (SpMet), total hemoglobin concentration (SpHb), and/or respiratory rate (RRac).

