EUDAMED Device Search & Export

Extract FDA medical device UDI records for device identification, product-code enrichment, manufacturer intelligence, and compliance workflows.

EUDAMED Medical Device Companies Scraper

scrapers_lat/eudamed-medical-device-actors-scraper

Directory of EU EUDAMED-registered medical device operators: manufacturers, authorised reps, importers and pack producers with email, phone, EU VAT, EORI, trade register number and named regulatory-compliance contacts. JSON, CSV, Excel.

EUDAMED Device Registration Change Monitor

xtech/eudamed-device-change-monitor

𝗠𝗼𝗻𝗶𝘁𝗼𝗿 𝗘𝗨𝗗𝗔𝗠𝗘𝗗 device registrations by UDI-DI, Basic UDI-DI, or exact trade name. Build a baseline, detect new or changed public records, and export manufacturer, status, changed fields, timestamps, and official source links.

Scrape EU-registered medical devices from EUDAMED (2.6M+). Device, risk class, status, manufacturer & EU authorised representative. MDR/IVDR compliance & medtech leads. Free, no key, no proxy.

FDA Device Recall Intelligence

skootle/fda-device-recall-intelligence

Official openFDA medical device recalls with product codes, device classes, K numbers, firms, root causes, actions, API output, schedules, monitoring, and integrations.

EUDAMED Certificates Scraper

automation-lab/eudamed-certificates-scraper

Export public EUDAMED MDR/IVDR certificate records with status, validity dates, manufacturers, notified bodies, and source URLs.

EUDAMED Scraper - EU Medical Devices, MDR & IVDR

perceptr0n/eudamed-medical-device-scraper

Export devices, manufacturers and notified-body certificates from EUDAMED, the EU's mandatory medical device registry. Risk class, market status, sterility, latex and CMR flags, market availability per country, CND codes and warnings — codes resolved to plain language.

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.

FDA 510(k) Clearances Scraper — Device Approvals

devilscrapes/fda-510k-clearances-scraper

Export openFDA 510(k) premarket device clearance records — applicant, device name, decision date and code, product code, advisory committee, device class and regulation number — filterable by applicant, device, product code, committee, class or decision-date range, as clean JSON, CSV or Excel.

openFDA Medical Device Adverse Events & Recalls Scraper

scrapers_lat/openfda-device-events-scraper

Scrape FDA medical device adverse events (MAUDE), device recalls and 510(k) clearances from the official openFDA API. Extract report number, device brand, manufacturer, event type, product problems and dates across the United States. Export to JSON, CSV or Excel.