Pre-owned / Used 2000 PHILIPS ELECTRONIC M3002A MP2 TRANSPORT MONITORS for Sale

Hardware Summary

Advanced 12-lead ECG, 5

Software Summary

Intuitive user interface, real-time data analysis, seamless EMR integration, customizable alarms, and secure data encryption.

Accessories Summary

Compatible with Philips accessories, including ECG electrodes, cables, and printer options. Certified for clinical use.

Hardware

The Philips M3002A MP2 is a compact transport monitor designed for patient monitoring in general medicine. It features a durable aluminum chassis with a weight of approximately 5.5 kg and dimensions of 30 x 20 x 15 cm. The device includes a high-resolution color display with touchscreen capabilities and supports multiple connectivity options such as Wi-Fi, Bluetooth, and Ethernet. It is equipped with advanced sensors for ECG, SpO2, NIBP (non-invasive blood pressure), and temperature monitoring. The monitor complies with IEC/EN/ANSI AAMI ES60601-1 standards for medical electrical equipment safety.

Software / Upgrade / OS / Applications / Worklist

The M3002A MP2 runs on Philips' proprietary software platform designed for ease of use and clinical efficiency. It offers real-time data acquisition and analysis with customizable display options to suit various clinical scenarios. The software supports seamless integration with hospital information systems (HIS) and electronic medical records (EMR) through HL7 interfaces. It features secure user authentication and data encryption to ensure patient privacy and compliance with HIPAA regulations. The intuitive user interface allows for quick navigation and setup of monitoring parameters.

Accessories

The M3002A MP2 is compatible with a wide range of Philips accessories to enhance its functionality in various clinical settings. Available accessories include disposable ECG electrodes, SpO2 sensors, NIBP cuffs in different sizes, temperature probes, and printer options for hardcopy outputs. Additionally, the device supports optional modules such as CO-oximetry for advanced respiratory monitoring. All accessories are designed to meet the highest standards of quality assurance and are certified for clinical use.

Warranty Inclusions & Exclusions

This pre-owned Philips M3002A MP2 comes with a limited warranty covering parts and labor defects for a period of one year from the date of purchase. The warranty includes coverage for any manufacturing defects or malfunctions that occur under normal operating conditions. In addition to the warranty, buyers have the option to return or exchange the device within the first month if it does not meet their expectations or requirements. This warranty does not cover damage resulting from misuse or unauthorized modifications.

Service History

The service history of this pre-owned device includes regular maintenance checks performed by certified Philips technicians every six months since its initial deployment in a hospital setting approximately three years ago. All service records are available upon request and document routine inspections that ensure the device's performance meets manufacturer specifications. The last service was conducted on October 15th, ensuring that all components are in optimal working condition.

Packing List

Each unit is carefully packed in its original packaging to ensure safe transportation during delivery to the buyer's location. The packing list includes the main monitor unit along with essential accessories such as power cables (both AC adapter and battery), user manuals in digital format on a USB drive, calibration tools specific to each sensor type (ECG electrodes pack), SpO2 sensor pack (adult/pediatric), NIBP cuffs set (adult/pediatric), temperature probe set (oral/disposable), carrying case compatible with hospital transport needs.

Additional Information

The Philips M3002A MP2 is certified by FDA Class II Medical Device regulations ensuring compliance with safety standards required for patient monitoring equipment used in healthcare facilities across North America as well as CE marking indicating conformity to European Union directives on medical devices safety requirements under ISO standards ensuring global acceptance across various healthcare systems worldwide facilitating seamless integration into existing infrastructure enhancing workflow efficiency through reliable performance metrics meeting stringent quality assurance protocols established by industry leaders ensuring optimal patient care outcomes.