Philips M8002A MP30 Intellivue Critical Care Patient Monitor M.04.05 Certified
Philips M8002A MP30 Intellivue Critical Care Patient Monitor M.04.05 Certified is backordered and will ship as soon as it is back in stock.
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Philips M8002A MP30 Intellivue Critical Care Patient Monitor M.04.05 Certified
Philips M8002A MP30
• Model: M8002A
• SW Version: M.04.05
• Weight: 15 lbs
• Monitor screen display: one integrated 26 cm (10.4") color SVGA
• Comfortable handle and rugged housing for easy portability.
• Screen Navigation: Touchscreen, navigation point compatible
• Waveforms: Three (four, six optional)
• Dimensions: 12" x 14-1/2" x 9"
Certified by Qualified Service Entity (CQSE):
This medical equipment item has been certified by a service entity skilled or trained to work specifically on this type of device. The certification process may involve repair with replacement parts, calibration, and the periodic maintenance recommended by the original manufacturer. Additionally, cosmetic work and cleaning may have been performed to enhance the visual appeal of the equipment. This ensures that the equipment not only meets operational standards but also maintains a visually pleasing appearance.
The Philips IntelliVue MP30 (M8002A) is a compact bedside monitoring platform designed for use in professional healthcare environments. The unit features a color LCD display, front-panel navigation controls, and an integrated handle for bedside or transport workflows. Its form factor supports use on carts, shelves, or mounted configurations depending on setup.
This monitor serves as a central display and processing unit for compatible external modules and accessories. It is intended to present physiological data when connected to appropriate inputs but does not perform independent diagnostic or therapeutic functions. No patient-applied accessories, sensors, cables, batteries, or mounting hardware are included unless explicitly stated.
The device powers on and is identified with software revision M.04.05. Certification or refurbishment references reflect inspection or testing status only and do not imply manufacturer recertification. Configuration, compatibility, and clinical suitability are the responsibility of the end user prior to deployment.

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