MedTrak offers an unparalleled platform to ensure the safety, efficacy, and lifecycle management of your implantable devices.
Streamlined Communication
Effortlessly share updates, recall notices, and maintenance requirements with device users and healthcare providers.
Regulatory Compliance
Simplify adherence to stringent reporting and tracking requirements with our secure and transparent system.
Enhanced Patient Engagement
Build trust and loyalty by empowering consumers with critical information and seamless device support.
Data Insights
Leverage anonymized data to gain valuable insights into device performance and real-world outcomes.
Recall Support
Ensure swift and efficient communication during FDA recalls. MedTrak’s platform helps you notify affected users instantly and provide them with clear, actionable steps to address the issue, protecting both your reputation and patient safety.
The Manufacturer Experience
1
A representative logs a procedure in MedTrak. It's as easy as scanning the device's barcode and selecting the patient, physician, and institution.
2
After the procedure, device tracking forms are sent to the institution and all relevant parties. No more endless paper copies to keep track of.
3
In the future, a manufacturer administrator initiates a recall from the MedTrak web application, and all patients, providers, and institutions affected by the recalled UDI numbers are notified instantly.
Join the MedTrak Revolution
Partner with MedTrak to innovate and elevate your device management strategies. Together, we can set a new standard in patient care and device safety.
