Pricing

from $20.00 / 1,000 maude event results

Go to Apify Store

FDA MAUDE Device Event Monitor

Try for free

Monitor medical device adverse events from openFDA MAUDE data.

Pricing

from $20.00 / 1,000 maude event results

Rating

0.0

(0)

Developer

Technical Dost Solutions

Actor stats

Bookmarked

Total users

Monthly active users

3 days ago

Last modified

Why this can sell

Store gap checked: FDA MAUDE had very low direct supply compared with device-risk demand.
Buyer intent is commercial: compliance, security, legal, regulatory, or competitive-intelligence workflows.
The Actor uses stable public APIs or official public feeds, so it can run on schedules without expensive browser proxy overhead.

Input

Run with the defaults for a sample dataset. Narrow the query fields for production monitoring.

Output

The default dataset contains normalized records with these fields:

reportNumber
eventType
dateReceived
manufacturerName
deviceName
productCode
patientOutcome
sourceUrl

Monetization

Best fit: pay per adverse-event row for medtech risk teams and consultants.

Notes

This Actor is designed as a reliable data product, not a brittle webpage scraper. Always validate regulated or legal data against the linked source before making business decisions.

FDA Medical Device Adverse Event Search (MAUDE)

ryanclinton/fda-device-events

Search the FDA's **MAUDE database of 24 million+ medical device adverse event reports** — including malfunctions, injuries, and deaths. Filter by device name, manufacturer, product code, event type, report number, or date range.

Ryan Clinton

openFDA Medical Device Events Scraper

parseforge/openfda-device-event-scraper

Export MAUDE medical-device adverse-event reports from openFDA. Search 24M+ reports by device name, manufacturer, event type, and event-date range. Pull report ID, device, manufacturer, event narrative, patient outcome, and dates.

ParseForge

Healthcare Compliance MCP — AI Agent FDA Device Intelligence

red.cars/healthcare-compliance-mcp

Query FDA MAUDE adverse events, 510(k) clearances, and device recalls. One tool call for AI agent medical device compliance research.

AutomateLab

FDA MAUDE Intelligence MCP

red.cars/fda-maude-intelligence-mcp

Medtech peer benchmarking intelligence for AI agents. Compare device manufacturers safety profiles against product-code peers using FDA MAUDE, 510(k), and enforcement data.

AutomateLab

FDA Medical Device Recall Search

ryanclinton/fda-device-recalls

FDA Medical Device Recall Search queries the U.S. Food and Drug Administration's openFDA device enforcement endpoint to retrieve detailed, structured data about medical device recalls.

Ryan Clinton

Medical Device Alert Monitor

zentrafoundry/medical-device-alert-monitor

Medical-device field safety notices, market-surveillance signals and device-risk tags.

Zentra

FDA Drug & Device Data Scraper (OpenFDA)

compute-edge/fda-openfda-scraper

Extract FDA drug approvals, adverse events, recalls, device clearances, and food recalls from the OpenFDA API. Search across 44M+ records with OpenFDA query syntax.

Compute Edge

5.0

openFDA Drug & Device Data Crawler

jungle_synthesizer/openfda-drug-crawler

Crawl FDA drug adverse events, recalls, labels, NDC codes, device events, and 510(k) clearances from the openFDA API. Filter by drug name, manufacturer, date range, and severity. 20M+ adverse event reports available.