BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    DISPOSABLE HIGH PRESSURE STOPCOCK/MANIFOLD MODEL HP STOPCOCK, MP STOPCOCK, HP MANIFOLD, PHP MANIFOLD

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973547·

    NEODENT GRAFT SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    SROM STM ST,36+6L NK,11X16X150

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·April 15, 2021

    MONOSYN UNDYED 3/0 (2) 45CM DSMP13 (M)

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·June 20, 2025

    SARA 3000

    FDA Adverse Event
    Injury ·MEDIBO N.V.·Product code FSA·November 24, 2008

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·May 21, 2013

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

    SAFESHEATH II 9F

    FDA Adverse Event
    Malfunction ·OSCOR INC.·Product code DYB·August 10, 2022