Adverse-event reports (MAUDE)
Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.
No adverse-event reports are linked to this device.
Recall history
No recalls linked.
Regulatory clearances
None linked.
Manufacturer compliance record
None in the loaded window.
Similar devices
- 12G-SDI cable OLYMPUS MEDICAL SYSTEMS CORP.
- 12G-SDI cable 1.5M OLYMPUS MEDICAL SYSTEMS CORP.
- 12G-SDI cable 8.5M OLYMPUS MEDICAL SYSTEMS CORP.
- 3G-SDI cable 1.5M OLYMPUS MEDICAL SYSTEMS CORP.
- AED NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
- AED Solar 2010 Portable LED Light Source NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
- AED Solar 4500 50-Watt LED Light Source NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
- AIR MICROPHONE OLYMPUS MEDICAL SYSTEMS CORP.
- BR Surgical, LLC BR Surgical, LLC
- BR Surgical, LLC BR Surgical, LLC
- BR Surgical, LLC BR Surgical, LLC
- BR Surgical, LLC BR Surgical, LLC
Select up to two to place side-by-side with this device.