Athera Healthcare’s MDR Solution: Driving Better Medical Device Outcomes

Athera Healthcare’s MDR solution is designed to help you maintain full compliance with the latest Medical Device Regulation (MDR) and MDOR requirements. Our advanced system enables healthcare providers to track and manage medical devices with patient safety as the top priority.

With comprehensive traceability of any implant used on a patient, our MDR solution ensures that you can respond quickly and effectively to any safety alerts or device recalls. This proactive approach supports better medical device outcomes, enhancing both patient care and overall healthcare experience for your patients.

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Our customers

What our customers say

“We haven't had a surgery cancellation due to inefficiencies within SSD for 3/4 years now... thanks to process improvements built from FingerPrint’s tech.”


Head of Sterile Services & Trust Decontamination Manager

Royal United Hospitals Bath NHS Foundation Trust

“I’ve used many traceability systems in the past and FingerPrint is by far the most user-friendly system – it’s so simple and easy to update, scan barcodes and see what’s going on across the full cycle”


CSSD Manager, Dublin Dental University Hospital

Athera FingerPrint

How Our MDR & MDOR Solutions Support Compliance

By automating device tracking, linking devices to patient records, and providing real-time updates, FingerPrint transforms how medical devices are managed in your hospital. This comprehensive system gives you a seamless approach to manage traceability, reporting, and recall processes.

Ensure Compliance

Automate data capture and reporting for MDR and MDOR, providing you with the assurance you’re meeting the latest regulations.

Reduce Risk

With real-time tracking and traceability, you can quickly respond to recalls and track devices to specific patients, reducing potential risks.

Repurpose your time

Automate the process of scanning, recording, and uploading device data, freeing up time for your team to focus on patient care.

Reduce the risk of human error

Automate data entry and use validated sources to ensure accuracy in every step, preventing manual entry errors that could lead to compliance issues.

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Discover how we can support you as the NHS navigates the new MDOR regulations
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Real-World Impact of MDR & MDOR Solutions

Supporting Better Medical Device Outcomes

How can FingerPrint support your team to ensure progress and continuous improvement?

  • Faster, More Accurate Reporting
  • Improved Governance & Assurance
  • Increased Efficiency
  • Stronger Patient Safety

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POWERFUL FEATURES

Improving Medical Device Outcomes with Data-Driven Insights

We know how difficult it can be to stay up-to-date with the latest regulations, which is why we’re always working with our customers to evolve with you. Our MDR solution was developed alongside healthcare professionals to proactively ensure we’re ready for the changes.

Scan Devices at Point of Care

At the moment of use, FingerPrint scans the UDI (Unique Device Identifier) barcode on medical devices, linking them directly to the patient.

Real-Time Data Capture

Capture essential device information (such as classification, batch number, and manufacturer) from trusted, validated sources like GoodID and GMDN.

Automatic data reporting

Device data is automatically uploaded to MDOR and other relevant registries, eliminating manual reporting and ensuring that your hospital meets legal requirements.

Full traceability

If a recall occurs, FingerPrint makes it simple to trace devices back to individual patients, enabling faster, more accurate responses to potential safety concerns.

Multi-barcode scanning

Scan multiple barcodes at once, reducing the time spent entering data and improving operational efficiency.

Seamless integration

Integrate with your existing hospital systems, ensuring smooth data flows. If we don’t currently integrate with a system you’d like to, our team are on hand to discover the best way to move forward.

Classified device data

FingerPrint uses the latest device classifications (like GMDN) to make sure you’re handling high-risk products according to MDR guidelines.

Automated Reporting

FingerPrint eliminates the need for manual data entry, automatically generating reports for MDOR.

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