Mindray MPM Masimo Set Mortara Module SpO2/ ECG/ NIBP/ 2-IBP 2-Temp V 2.0 115-022715-00

Mindray 115-022715-00 MPM Masimo Mortara Set Module SpO2/ ECG/ NIBP/ 2-IBP 2-Temp V 2.0 Certified

• Model: 115-022715-00
• SpO2, ECG, NIBP, 2-IBP
• 2-Temp
• Compatibile with Passport 12m, Passport 17m, DPM 6+ and DPM 7+ Patient Monitors
• Software Version: Ver2.0
• Weight: 2 lbs.
• Overall Length: 5-1/2 inches x 3 inches x 4 inches

This module is a multi‑parameter monitoring module designed to support comprehensive vital sign monitoring within compatible Mindray monitors (Passport 12m, Passport 17m, DPM6+, DPM7+). By packing together SpO₂ (via Masimo’s algorithm), ECG waveform and heart rate, non‑invasive blood pressure (cuff‑based), two invasive blood pressure channels, and two temperature channels, it delivers a high‑utility module for critical care, postoperative, transport, or monitoring situations where multiple hemodynamic parameters are needed simultaneously. The “Mortara Set” name suggests it adheres to certain standards of ECG/SpO₂/pressure channel fidelity often associated with Mortara’s calibration / interface norms, although in this case it’s a module for Mindray; the “V 2.0” indicates a firmware/software version with possibly updated features or bug fixes. The ability to monitor two separate invasive blood pressures allows clinicians to track both arterial and central venous pressure (or other dual sites), which is important in hemodynamic management.

Mechanically, the module’s form factor (≈ 5.5″ × 3″ × 4″, weighing about 2 lbs) makes it a sizable plug‑in module. It occupies one module slot in the host monitor, interfacing for power, data, alarm integration, etc. The dimensions make consideration for insertion/removal, cooling, mounting, and cable routing relevant—since IBP lines and temperature probes add external connections. It likely includes internal isolation, signal conditioning, and safety features to meet standards for medical electrical equipment, especially because invasive lines pose risk if there is leakage or signal error. Calibration and certification are mentioned in the listing (“certified”) so this particular unit has likely been tested for accuracy, and cosmetic cleaning and calibration have been done to ensure operational readiness.

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.