Philips Intellivue X2 Patient Monitor

Philips Intellivue X2 Patient Monitor

The Philips Intellivue X2 is a compact, portable patient monitor designed for multi-parameter vital signs monitoring at the bedside, during transport or in step-down clinical environments. This unit is offered pre-owned and carries product code M3002A.

What is included

What is not included

Checked before dispatch

• Unit cleaned and inspected visually for physical damage
• Function tested to confirm screen operation and basic system startup
• These are in-house workshop checks. Damaged or non-working units are not dispatched.
• A full engineer service and calibration is not included unless this listing states the unit has been serviced.
• This item may require service and calibration before clinical use. Planned maintenance, periodic electrical safety testing and medical device verification remain with the operating organisation.

Compatibility

The Intellivue X2 is designed to operate as a standalone portable patient monitor and as a companion module with compatible Philips Intellivue host monitors, including the MP30, MP50 and MP70 series. When used as a companion module, a host interface cable is required and is sold separately. Confirm compatibility with your existing infrastructure before ordering.

Consumables and patient-contact items

ECG cables, SpO2 probes, blood pressure cuffs and all other patient-contact consumables are single-use or require decontamination and inspection before reuse. None are included. Source replacements through your clinical supplies department or ask before ordering if you need compatible part references.

Photographs

Photographs form part of the description. Review all images before purchasing. If additional photographs of a specific area are needed, ask before ordering.

Regulatory note

This is a pre-owned medical device. The receiving organisation is responsible for incoming inspection, electrical safety testing and any service or calibration required before the unit is placed in clinical use. PUWER 1998 applies to powered medical equipment in workplace settings. Verify that local decontamination protocols have been followed to a standard appropriate for the intended clinical environment.

Information on this page is provided for guidance and does not replace advice from a qualified clinician. Always read the manufacturer's instructions before use, and check that a device is suitable for the patient and the prescribed therapy.