No-Code Studio
Medical device types with the fields your regulator expects.
Mintema is medical equipment management software. Register every device with its regulatory class, location and service history, plan preventive maintenance and calibration, and record safety tests and recalls.
Thousands of devices need preventive maintenance, calibration and safety tests, while recalls and accreditation need evidence. Without one record, readiness depends on memory.
Every part below is configured in the platform without code: the asset type, its structure, the inspection form and scoring, the work, the sensors and the dashboards. Click a step, or let it play.
A designed type with regulatory class, manufacturer, model, serial, risk class and calibration interval.
Hospital, building, department and room, with each device and its accessories.
Leakage current, earth resistance and performance readings, with technician and supervisor signatures.
Planned PPM and calibration orders by device class; faults reported by wards become corrective orders.
Medical refrigerators and gas systems report temperature, pressure and alarms.
Inspection compliance, maintenance backlog and audit readiness per hospital.
Illustrative configuration on sample data. Your fields, forms, scales and workflows are designed with your team.
One platform and one data model, so the inspection, the work order, the spare part, the sensor and the dashboard all refer to the same asset.
Medical device types with the fields your regulator expects.
Safety and performance tests with signatures.
PPM, calibration, faults and recall actions.
Medical fridges and gas systems monitored.
Accreditation and compliance reports on schedule.
Full service history per device.
The value is measured in fewer failures, less wasted effort, lower risk and better use of budget.
Have a question that is specific to your organisation? A solution engineer will answer it against your own assets, processes and data.
Medical equipment management software, also called clinical engineering software, keeps a register of every device with its class, location, maintenance, calibration, safety tests and recalls.
Yes. The medical device type is designed in the No-Code Studio with the fields you need, including regulatory class, model and serial number.
Yes. Test forms combine checklists, measurements and signatures, and approval can require a supervisor.
Devices are found by model and serial, and recall action work orders track each device to completion.
Yes. Each hospital is an organisation in the tree, with its own users and devices, and a group-wide view for management.
A recall is matched to the affected devices by model and serial number, work orders are raised for each, and the closure evidence is kept.
Yes. Test forms record readings against limits with a pass or fail, and results attach to the device history.
We will configure this use case on sample data during the call: the asset type, an inspection form with its scoring, a work order type and a rule.