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Export breast implant rupture reports (MAUDE)

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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FDA Adverse Events Scraper - FAERS + MAUDE Export
FDA Adverse Events Scraper - FAERS + MAUDE Exportmaydit/us-fda-adverse-events-scraper
Type
Report #
Received
Serious
+9 fields
Text
Number
Boolean
List
Object

Input

Report type:device
Product name:breast implant
Reaction / product problem:Material Rupture

Output fields

Type
Report #
Received
Serious
Event
Product(s)
Generic
Manufacturer
Reactions
Problems
Age
Sex
Country

How it works

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.

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