BEUDAMED
    12 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    EXULT Knee Replacement System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·April 20, 2026

    Suture Wires and Wire Loops

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FIBRIN ANALYSIS SYSTEM ENDOLUMINAL BRUSH

    FDA 510(k)
    FDA Class 2 ·General Hospital

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 1, 2026

    LD304 MATERNITY BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code HDD·May 29, 2015

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FOZ·April 6, 2026

    GPS PROCEDURAL STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·December 2, 2008

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·September 16, 2011

    SNAP-FIT PADDLE BLADE ACCESSORY

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 29, 2013