BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    MEDTRONIC VASCULAR CATHETER, MULTI LUMEN MODELS 84640, 84652

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VSI StraitSet micro-introducer kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BAND-AID BRAND PLASTIC BANDAGES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SPIROPERFECT

    FDA Adverse Event
    Malfunction ·MEDIKRO OY·Product code BZG·August 11, 2023

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 20, 2010

    2520274-2013-10054

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code KWQ·February 11, 2013

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 28, 2014

    UNKNOWN REDAPT HIP ACETABULAR IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code LPH·September 18, 2023