Export breast implant rupture reports (MAUDE)
Brandt May
Returns the 50 FDA MAUDE device reports most recently received by the FDA for breast implants that list the product problem Material Rupture. Each row gives the implant brand and style, generic device name, manufacturer, event type, the reported device problems and the received date. Used by plastic surgery practices, device-safety researchers and product-liability law firms.
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Sign up on Apify01
Create your Apify account to access the FDA Adverse Events Scraper - FAERS + MAUDE Export.
Start the run02
The Actor will start running based on the input automatically.
Receive the output03
Monitor the progress in real-time. You will be notified as soon as your dataset is complete and ready for review.
Integrate into your workflow04
The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow.
