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

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    BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471130500·K-WIRE - DOUBLE TROCAR WITH GUIDE 0.9mm DIA x 1...

    FRAG-LOC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM TRIMETHOPRIM - GN 0.5-16 UG/ML

    FDA 510(k)
    FDA Class 2 ·Microbiology

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·January 28, 2013

    PFC SIGMARP CV TB/IN S3 10.0

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code NJL·December 14, 2010

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 13, 2014

    TOTAL ABSCESSION DRAINAGE CATHETER

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS, INC.·Product code GBX·November 14, 2007