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MEMIS

MEMIS

Healthy

Medical equipment management software streamlines equipment maintenance and oversight. Enabling easy to access asset registry. Ensuring risk management, compliance, and patient safety. Commonly used by, but not limited to, clinical engineering, IT, radiology, lab, dental, home care

Many healthcare organisations require the capability to access their medical equipment across multiple facilities and departments. Medical equipment management software with cloud-based deployment can make it seamless for healthcare organisations to track maintenance requests across large distances. At the same time, a medical equipment management solution will provide clinical engineers improved asset visibility compared to an Excel spreadsheet.

A few medical equipment management solutions also extend accessibility to mobile applications, making it easy to access while on the go. Some solutions can be deployed locally at the facility, allowing for offline capabilities that will allow hospital staff to document information while disconnected from the internet.

MEMS Asset Registry & Management

MEMS Asset Registry & Management

Asset Registry & Management

Asset Registry & Management

Medical equipment management software (MEMS) is ultimately a tool to streamline management of healthcare assets. Compared to various other industries, in the healthcare industry it is crucial that all medical equipment, assets, and devices is maintained in an excellent condition to ensure patient safety.

Especially, high risk and high device class medical equipment, such as defibrillators and ventilators, must follow strict maintenance. It is critical that these tools are in top condition and available to physicians, nurses, and other hospital staff.

Regulatory Compliance of Medical Devices

Regulatory Compliance of Medical Devices

Regulatory Compliance of Medical Devices

Regulatory Compliance of Medical Devices

Medical equipment management software plays an important role managing preventive maintenance of all medical equipment, reducing the potential risk of equipment failure, and providing analytics.

Depending on your location there are various compliance that needs to be followed such as: Global medical device nomenclature (GMDN), European database on medical devices (EUDAMED), European medical device regulation (MDR), and unique device identification (UDI).

Internal Review in Healthcare Organisations

Internal Review in Healthcare Organisations

Internal Review in Healthcare Organisations

Internal Review in Healthcare Organisations

Many healthcare organisations require internal review and may request reports related availability of medical devices, downtime, amount of planned preventive maintenance the coming quarter, amount of unplanned maintenance, and work order turnaround times, only to mention a few. This information will be used in decision making and investment processes, while also helping clinical engineering to balance and quantify part of their workload.