BEUDAMED
    73 results · 24ms · Sources: EU EUDAMED, US FDA

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    R501 aortic root cannula without vent line, R502 aortic root cannula with vent line

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VITA TITANKERAMIK

    FDA UDI
    Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft·J017B2006120·VITA TITANKERAMIK OPAQUE, B1, 12 g

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377047670·RELINE-O Trial, 8mm H Ang Right L-pop

    Ceramco® iC

    FDA UDI
    Dentsply International Inc.·D00142006120·C3

    ARCHITECT I1000SR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·August 31, 2022

    Zavation

    FDA UDI
    Zavation LLC·00842166131767·Ti3Z CIF 12mmx14mmx12mm -6 deg

    VERSANT LEVI

    FDA UDI
    FGX INTERNATIONAL INC.·00193033308325·

    Apelo® / Apelo® MIS

    FDA UDI
    ATLAS SPINE, INC.·M68120061200000·Marker Inserter Sleeve

    SULTAN SPOROX TEST VIAL, MODEL 75195

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TRAY 40CM PERMCATH

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/KENDALL·Product code LFJ·December 22, 2006

    SYNCHROMED II

    FDA Adverse Event
    Other ·MEDTRONIC·Product code LKK·June 12, 2006

    FOGARTY

    FDA Adverse Event
    Other ·EDWARDS LIFESCIENCES·Product code DXE·July 17, 2006

    UNK

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·April 20, 2006

    INVERNESS EAR PIERCING SYSTEM

    FDA Adverse Event
    Other ·INVERNESS CORPORATION·Product code JYS·July 25, 2007

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Death ·PHYSIO-CONTROL, INC.·Product code MKJ·September 23, 2010

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 19, 2008

    DEEP BRAIN STIMULATOR LEAD

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·February 19, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 19, 2008

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 22, 2007