BEUDAMED
    1,141 results · 24ms · Sources: EU EUDAMED, US FDA

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    X-Tack Endoscopic HeliX Tacking System

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

    DJO SURGICAL

    FDA UDI
    Encore Medical, L.P.·00190446932369·SPECIAL, DAA DBL OFFSET BROACH HANDLE, EMPOWR B...

    HHM

    FDA UDI
    Oticon A/S·05707131355263·G300 SC, MINIRITE T 312 2.4G C090 HHM

    NA

    FDA UDI
    Synthes GmbH·10886982142917·2.0MM CORTEX SCREW SELF-TAPPING 8MM

    NA

    FDA UDI
    Stryker GmbH·07613154639687·Screw Marker 18,8

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383549271·"An absorbent paper points is an endodontic pap...

    DORO HEADREST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·August 22, 2018

    HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·April 5, 2018

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·May 4, 2018

    HEARTWARE VENTRICULAR ASSIST SYSTEM - BATTERY

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·September 11, 2018

    HEARTWARE VENTRICULAR ASSIST SYSTEM - BATTERY

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·August 13, 2018

    ARCTIC SUN 5000

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·September 10, 2019

    ALARIS INFUSION PUMP

    FDA Adverse Event
    Injury ·CARDINAL HEALTH ALARIS PRODUCTS·Product code FRN·October 15, 2008

    GENESISXP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 26, 2013

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·August 5, 2011

    HEARTWARE VENTRICULAR ASSIST SYSTEM - BATTERY

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·August 16, 2018

    HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·March 23, 2018

    IFUSE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·SI-BONE, INC.·Product code OUR·July 28, 2017