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moorVMS-TREND PC Software

MOOR INSTRUMENTS LIMITED · Model 1 · UDI-DI 15060484490164

MUDGEX Prescription
2
510(k) clearances
738
Adverse events (6 deaths)
6
Recalls
58
Facilities

Description

moorVMS-TREND PC software is intended for use with moorVMS-LDF and moorVMS-OXY, for long term blood flow and tissue oxygen trend monitoring. It is intended for a variety of physiological and clinical research applications in clinical settings. The clinical value of measurements in disease states has not been established. The moorVMS-TREND is not intended to be used as the sole basis for diagnosis or therapy. The moorVMS-TREND Software is not intended for critical care monitoring where loss of function could result in harm to the patient.

Recalls

DateFirmReason
2024-01-09Covidienmanufacturing defects to sensor cable connectors may result in error codes or non-functioning channel
2024-01-09Covidienmanufacturing defects to sensor cable connectors may result in error codes or non-functioning channel
2023-10-30KENT IMAGING, INC.Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation images.
2022-03-01Edwards Lifesciences, LLCThe StO2 values may be inaccurately low when using either the FORE-SIGHT ELITE Tissue Oximeter Module or the FORE-SIGHT ELITE Absolute Tissue Oximeter Monitor with the Fore-Sight E
2022-03-01Edwards Lifesciences, LLCThe StO2 values may be inaccurately low when using either the FORE-SIGHT ELITE Tissue Oximeter Module or the FORE-SIGHT ELITE Absolute Tissue Oximeter Monitor with the Fore-Sight E
2009-10-23Nonin Medical, IncA malfunction was detected with one of the components that, under rare circumstances, may result in the overheating of the POD. This overheating, while unlikely to occur, has the

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.