Mastering Medical Device Data

MAUDE alternative

The most up to date information on adverse events involving medical devices

Attorneys and legal

Comprehensive Medical Device Data needed to support the case.

Wealth management

Health Information Technology – Medical Device Financial Forecasting.

Hospitals and doctors

Improve Patient Outcomes & Reduce Risk Through Better Information.

Innovative solutions

Looking for superior Search and Reporting alternative to MAUDE?

Device Events is a cloud-based software service that provides fast, easy-to-use, comprehensive and cost-effective access to the most up-to-date information on adverse events involving medical devices.

Who we are

The MAUDE Solution

MAUDE – The Manufacturer and User Facility Device database platform is antiquated and difficult to use.

DEVICE EVENTS provides an alternative cloud-based software service that extracts, consolidates and provides clear and comprehensive metrics and reports on the millions of complex medical device adverse event reports (MDRs) and recalls that have been filed with the FDA.

A device report as shown in Device Events The same report as shown in the FDA MAUDE database

Use the slider above to note changes between programs.

Get the right data – use Device Events.

Key Features

Fast Search & Retrieve from the FDA MAUDE Database | Trend Visualizations | Email Notifications

Register

Signals is a Quarterly Newsletter on the latest medical device adverse event news, information and trends.

Demonstration

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Get the right data – use Device Events.

Software Features

Device Events is a cloud-based software service that extracts, consolidates, and provides comprehensive information on the millions of FDA medical device adverse event reports (MDRs). You can access the system at your convenience once you have account login credentials.

The system provides you with fast and cost-effective access to the most up-to-date information available – so you can quickly identify problem devices, understand the history, quantity and severity of the related adverse events and make better, more informed decisions.

The Device Events system will improve the quality of your research while reducing the amount of time you spend on that research. The result is improved patient safety, better health outcomes, and reduced risk for healthcare organizations.

Association

Trusted and Supported

  • Former FDA Unique Device Identification (UDI) External Program Manager
  • Former FDA Adverse Events Project Manager for Devices (MAUDE)
  • Medical Device Epidemiology Network (MDEpiNet) UDI Think Tank
  • MDEpiNet National Medical Device Registry Task Force & Catalog Number Workgroup

Get the right data – use Device Events.

Join Now!

Join today and enjoy the many benefits the Device Events Database offers. Time is key, do not waste yours using out of date software.

Contact Us

Contact us to learn more about Device Events database search capabilities.