BEUDAMED
    10 results · 24ms · Sources: EU EUDAMED, US FDA

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    KERRISON RONGEURS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Cathivex ¿GV filter units

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CHARLOTTE SNAP-OFF SCREW, MODELS 45110001, 45110002, 45110003

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HL20 BUBBLE SENSOR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTQ·January 30, 2015

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·April 30, 2014

    SCANLAN MICRO CLAMP

    FDA Adverse Event
    Other ·SCANLAN INTERNATIONAL, INC.·Product code DWS·December 9, 2010

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 9, 2013

    BD SAFE-CLIP¿ NEEDLE CLIPPING & STORAGE DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·September 25, 2019

    SHARPS DISPOSAL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·August 16, 2019

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021