One register for your medical equipment - with calibration and electrical safety due dates, failed devices quarantined automatically and manufacturer recalls traced to the exact serials on your wards.
Built for biomedical engineering
Everything the clinical engineering team and quality office need to prove every device is safe to use.
Medical device register
Risk class, GMDN / UMDNS code, regulatory registration, department and life-support flag on every device, with its full history.
Calibration schedule
Due dates calculated from each device's interval or its risk class, with measurements and certificate number for every calibration.
Electrical safety (IEC 62353)
Protective earth and leakage current measurements recorded per test, with the next test date set automatically.
Failed devices quarantined
A failed test quarantines the device and opens a work order - priority 1 for life-support equipment - until a passed re-test.
Recalls and safety notices
Enter a field safety notice once; the affected devices are found by manufacturer, model and serial, each with its own work order.
Compliance at a glance
Compliance rate, overdue calibrations and safety tests, devices due in 30 days, quarantined devices and open recalls.
Ready for your accreditation surveys
Surveyors ask for proof that every device was inspected on time. Teknora keeps that evidence in one place.
- Complete inventory of medical equipment with risk classification
- Planned maintenance and inspection schedule per device
- Calibration and electrical safety records with certificates
- Traceable action on manufacturer recalls and safety notices
- Quarantine and return-to-service evidence for failed devices
- Full audit trail of every status change
Live in a week
- Load your device register - Import from a spreadsheet or your current system - each device becomes an asset with its own history.
- Engineers record tests - From the workstation or a tablet at the bedside: measurements, result and certificate.
- Quality sees compliance - Overdue items, quarantined devices and recalls are visible the moment they happen.
Run a pilot on one department
We load your devices with you and train the biomedical engineering team.