ANGIOMED GMBH & CO. MEDIZINTECHNIK KG
Manufacturer adverse-event records for ANGIOMED GMBH & CO. MEDIZINTECHNIK KG come from the U.S. Food & Drug Administration (FDA) MAUDE database via openFDA, refreshed March 2026 - see our methodology. Not medical advice.
FDA MAUDE device safety record · 2001–2026 · thin-book · elevated Death-code · balanced
Volume signature
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG is a thinner MAUDE footprint
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG accounts for 4,906 FDA MAUDE reports (#364 of 443, thin-book tercile). Death-coded event_type share is 1.14% (elevated); Injury share 26.2% (balanced).
What the volume reading shows for ANGIOMED GMBH & CO. MEDIZINTECHNIK KG
The standout signal for ANGIOMED GMBH & CO. MEDIZINTECHNIK KG is filing volume: 4,906 adverse-event reports in FDA MAUDE (#364 of 443, thin-book). Death-coded event_type share sits at 1.14% (elevated).
As a thinner-book manufacturer, a handful of device families can swing the totals; open the device table rather than reading the company headline alone. Event_type counts are not the same population as Patient Outcomes.
Reports span 15 device types, led in this extract by Malfunction at 3,565 (72.7% of event_type total). Peak single-year volume reaches 697 reports across 26 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Devices (15)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.