PlainHospital

UNOMEDICAL UM-D

Manufacturer adverse-event records for UNOMEDICAL UM-D 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 · 2023–2026 · mid-book · quiet Death-code · balanced

Death-code intensity

UNOMEDICAL UM-D is quieter on Death-coded events

Death-coded event_type rows are 0 of 8,880 (0.00% · quiet tercile among 443 manufacturers). Absolute volume is mid-book.

What the Death-code reading shows for UNOMEDICAL UM-D

The standout signal for UNOMEDICAL UM-D is Death-code intensity: 0.00% of 8,880 reports (quiet tercile), while absolute volume is mid-book.

Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for UNOMEDICAL UM-D. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.

Reports span 2 device types, led in this extract by Malfunction at 7,467 (84.1% of event_type total). Peak single-year volume reaches 7,917 reports across 4 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

8,880
Total Reports
0
Event-type Death
1,413
Injury Reports
2
Device Types

Event Types

Malfunction 7,467 (84.1%)
Injury 1,413 (15.9%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

7,651 (80.5%)
Required Intervention 842 (8.9%)
Hospitalization 305 (3.2%)
R 291 (3.1%)
H 274 (2.9%)
L 65 (0.7%)
Life Threatening 51 (0.5%)
Other 12 (0.1%)
Disability 9 (0.1%)
O 7 (0.1%)
S 2 (0.0%)
Congenital Anomaly 1 (0.0%)

Devices (2)

Device Reports
Set, Administration, Intravascular 8,879
Cystometric Gas (Carbon-Dioxide) On Hydraulic Device 1

Yearly Trend

23
2023: 7
24
2024: 579
25
2025: 7,917
26
2026: 377

Read our methodology - how this data is sourced, computed, and verified.