MEDOS INTERNATIONAL SARL
Manufacturer adverse-event records for MEDOS INTERNATIONAL SARL 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 · 2015–2026 · mid-book · typical Death-code · balanced
Death-code intensity
MEDOS INTERNATIONAL SARL tracks a typical Death-code share
Death-coded event_type rows are 92 of 13,641 (0.67% · typical tercile among 434 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for MEDOS INTERNATIONAL SARL
The standout signal for MEDOS INTERNATIONAL SARL is Death-code intensity: 0.67% of 13,641 reports (typical tercile), while absolute volume is mid-book.
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for MEDOS INTERNATIONAL SARL. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 20 device types, led in this extract by Malfunction at 11,729 (86.0% of event_type total). Peak single-year volume reaches 2,369 reports across 12 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 (20)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.