PlainHospital

GE OEC MEDICAL SYSTEMS GMBH

Manufacturer adverse-event records for GE OEC MEDICAL SYSTEMS GMBH 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 · 2003–2014 · thin-book · quiet Death-code · injury-light

Injury-mix signature

GE OEC MEDICAL SYSTEMS GMBH is lighter on Injury codes

Injury-coded event_type share is 0.0% (injury-light tercile) beside 0.00% Death-coded (quiet). Volume band: thin.

What the Injury-mix reading shows for GE OEC MEDICAL SYSTEMS GMBH

The standout signal for GE OEC MEDICAL SYSTEMS GMBH is Injury-mix: 0.0% Injury-coded (injury-light) beside 0.00% Death-coded, on a thin-book footprint.

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 3 device types, led in this extract by Malfunction at 6,464 (100.0% of event_type total). Peak single-year volume reaches 2,268 reports across 9 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

6,465
Total Reports
0
Event-type Death
0
Injury Reports
3
Device Types

Event Types

Malfunction 6,464 (100.0%)
1 (0.0%)

Patient Outcomes

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

6,463 (100.0%)
Congenital Anomaly 1 (0.0%)
Other 1 (0.0%)

Devices (3)

Device Reports
System, X-Ray, Fluoroscopic, Image-Intensified 6,462
System, X-Ray, Tomography, Computed 2
System, Image Processing, Radiological 1

Yearly Trend

03
2003: 1
06
2006: 1
07
2007: 1
08
2008: 1
10
2010: 426
11
2011: 2,268
12
2012: 1,465
13
2013: 1,725
14
2014: 577

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