FDA adverse event reports for insulin pumps (MAUDE)

Created by

Timothy Kelvin

Actor

FDA MAUDE Search: Medical Device Adverse Events

Malfunction, injury and death reports involving insulin pumps received by the FDA in the last 90 days, with manufacturer, brand, event date and reporter type.

Try for free

FDA MAUDE Search: Medical Device Adverse Eventsm_ctim/medical-device-adverse-event-tracker

Report number

Event type

Date received

Date of event

+5 fields

Input

Device name:insulin pump

Event type:all

Days back:90

Max results:50

Output fields

Report number

Event type

Date received

Date of event

Device generic name

Device brand name

Manufacturer

Product problem flag

Reporter occupation

How it works

Sign up on Apify or log in

The FDA MAUDE Search: Medical Device Adverse Events Actor is ready to run with the inputs already set for "FDA adverse event reports for insulin pumps (MAUDE)". Sign up or log in and you'll land in Apify Console with a copy of this exact task.

Start the "FDA adverse event reports for insulin pumps (MAUDE)" task

The FDA MAUDE Search: Medical Device Adverse Events Actor will start running based on the input automatically. You can also change all the input fields, like device name, event type, and more, to match your specific use case.

Receive the "FDA adverse event reports for insulin pumps (MAUDE)" output

Monitor the progress in real time. You will be notified as soon as your dataset is complete and ready for review. Each result includes data such as report number, event type, date received, and more.

Integrate into your workflow

The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow. You can also run the "FDA adverse event reports for insulin pumps (MAUDE)" task via API.