BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Medline ReNewal Reprocessed Harmonic ACE+7 Shears

    FDA 510(k)
    FDA Unclassified ·Unknown

    EarQ

    FDA UDI
    Oticon A/S·05707131342829·G20, MINIRITE T 312 2.4G C092 EARQ

    PRECISION PORTABLE OXYGEN CONCENTRATION MODEL 4150

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IU22 ULTRASOUND SYSTEM AND TRANSDUCERS

    FDA 510(k)
    FDA Class 2 ·Radiology

    NEEDLE 23X1 RB

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·March 2, 2021

    BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·September 10, 2024

    BONE REDUCTION FORCEPS-LARGE

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTD·August 14, 2020

    SYNERGY

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·June 27, 2013

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·July 13, 2011

    PERFORMER BALKIN GUIDING SHEATH

    FDA Adverse Event
    Injury ·COOK INC.·Product code DYB·September 23, 2008