BEUDAMED
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    HUNTLEIGH HEALTHCARE LTD.

    FDA registration
    HUNTLEIGH HEALTHCARE LTD.·10 products·🇬🇧 United Kingdom

    SONICAID

    FDA Adverse Event
    Malfunction ·HUNTLEIGH HEALTHCARE LTD. DIAGNOSTICS·Product code HEL·April 11, 2013

    SONICAID

    FDA Adverse Event
    HUNTLEIGH HEALTHCARE LTD. DIAGNOSTICS·Product code HGM·October 26, 2012

    SONICAID

    FDA Adverse Event
    Death ·HUNTLEIGH HEALTHCARE LTD. DIAGNOSTICS·Product code HGM·February 8, 2012

    STREAMLINE CONTINENTAL B

    FDA Adverse Event
    Malfunction ·HUNTLEIGH HEALTHCARE LTD - AKRON·Product code FNL·September 1, 2011

    SONICAID

    FDA Adverse Event
    Injury ·HUNTLEIGH HEALTHCARE LTD·Product code HGM·February 17, 2016

    SONICAID

    FDA Adverse Event
    Death ·HUNTLEIGH HEALTHCARE LTD·Product code HGM·November 3, 2017

    PHYSIO COUCH

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH·Product code FRK·July 21, 2011

    SONICAID

    FDA Adverse Event
    Death ·HUNTLEIGH HEALTHCARE LTD. DIAGNOSTICS·Product code HGM·September 12, 2014

    SONICAID

    FDA Adverse Event
    Malfunction ·HUNTLEIGH HEALTHCARE LTD.·Product code HGM·November 14, 2011

    ACCESSORIES - MEDICAL BEDS

    FDA Adverse Event
    Malfunction ·HUNTLEIGH HEALTHCARE LTD.·Product code FNL·September 3, 2013

    NIMBUS 3/DFS3

    FDA Adverse Event
    Malfunction ·HUNTLEIGH HEALTHCARE LTD.·Product code FNM·August 23, 2013

    HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative Probes, REF DIOP8

    FDA Recall
    Terminated ·Huntleigh Healthcare Ltd.·Product code ITX·February 11, 2022

    HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative Probes, REF DIOP8

    FDA Enforcement
    Class II ·Terminated·Huntleigh Healthcare Ltd.·April 27, 2022

    PHYSIOTHERAPY COUCH

    FDA Adverse Event
    Malfunction ·HUNTLEIGH HEALTHCARE LTD - AKRON·Product code FQO·February 1, 2012

    SONICAID

    FDA Adverse Event
    Death ·HUNTLEIGH HEALTHCARE LTD, DIAGNOSTICS·Product code HGM·June 27, 2014

    SONICAID

    FDA Adverse Event
    Death ·HUNTLEIGH HEALTHCARE LTD., DIAGNOSTICS·Product code HGM·June 27, 2014

    COUCHES

    FDA Adverse Event
    Malfunction ·HUNTLEIGH HEALTHCARE LTD. - AKRON·Product code FMS·May 13, 2012

    SONICAID

    FDA Adverse Event
    Death ·HUNTLEIGH HEALTHCARE LTD. DIAGNOSTICS·Product code HGM·March 28, 2013

    SONICAID

    FDA Adverse Event
    Death ·HUNTLEIGH HEALTHCARE LTD. DIAGNOSTICS·Product code HGM·February 26, 2013