453564205181 PHiliph MX40 Patient Monitor Parts Rear Housing LOT 1667975

PHiliphh MX40 patient monitor rear housing 453564205181 LOT 1667975

Service personnel can find the following information on the label on the back of the MX40:

Service #: This is the Service Identification Number located on the back label and used to identify the device.

S/N: This is the Hardware Serial Number for the device located on the back label and used to identify the device.

SW SN: This is the Software License Number. It can be found on the Software License Certificate that shipped with the device.

Options: List of enabled product options on the device.

Declaration of intended use

It is designed to monitor, record and generate alarms for a wide range of physiological parameters in adults and children in the hospital environment and during patient transport within the hospital. not suitable for home use For use by healthcare professionals

User's Guide

It is recommended for use by healthcare professionals when monitoring the patient's physiological parameters. For monitoring, recording and alarming various physiological parameters. in adults and children in hospital settings and during intra-hospital transport.

Intended use MX40

The MX40 is primarily used as a traditional telehealth device. Connects Wirelessly to the IntelliVue Information Center When the MX40 is connected to the IntelliVue Information Center, the IntelliVue Information Center provides initial patient monitoring and alerting functions. When connected to the message center, the MX40 does not automatically perform local checks or notifications.

The MX40 can provide time-limited local monitoring when not connected to a wireless network. Unlike traditional AC night monitors, the MX40 is battery powered and cannot provide continuous monitoring.

Patient Population

This device is not intended for use on infants and newborns. Clinical judgment should be used to determine when MX40 should be administered to a particular pediatric patient, as ECG performance cannot be attributed to exact body weight or age. This device can only be used on one patient at a time. Parts/accessories that come into contact with the patient's skin meet the biocompatibility requirements according to EN ISO 10993-1. This device is not intended for direct contact with the patient's skin. The included bag is suitable for storing equipment.

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