BEUDAMED
    49 results · 61ms · Sources: EU EUDAMED, US FDA

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    Auxein Nailing System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PureLife+ Sterilization Pouches

    FDA UDI
    PURELIFE, LLC·D79011920031·PureLife+ Sterilization Pouches, 3 1/2" x 5 1/4...

    Bernafon

    FDA UDI
    Bernafon AG·05711584086773·ZR3, KIT 312 2.4G NFM L BE ZERENA 3

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776199791·LLETZ GRAVES SPEC SM WEVAC

    CETRA

    FDA UDI
    Orthofix US LLC·18257200137466·CETRA - 2.0 BOTTOM TRAY-LEVEL, IMPLANT/INSTRUME...

    XPRESS BALLOON DEVICE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    CPC SLEEP DATA RECORDER, MODEL M1, AND APPLICATION SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CATHETER PORTNOY VENTRICULAR STRIPED

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES INC.·Product code HCA·March 4, 2003

    BABY CONTROL WALL MOUNT INFANT WARMER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code FMT·March 20, 2011

    GUIDANT 4.5 MM HEARTSTRING PROXIMAL SEAL

    FDA Adverse Event
    Malfunction ·GUIDANT CARDIAC SURGERY·Product code DXC·September 10, 2003

    GUIDANT 4.5 MM HEARTSTRING PROXIMAL SEAL

    FDA Adverse Event
    Malfunction ·GUIDANT CARDIAC SURGERY·Product code DXC·September 10, 2003

    LIFESITE HEMODIALYSIS ACCESS SYSTEM

    FDA Adverse Event
    Injury ·VASCA, INC.·Product code MSD·March 19, 2003

    UCR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·SEASPINE, INC.·Product code KWP·February 5, 2004

    ALTO

    FDA Adverse Event
    Malfunction ·ELA MEDICAL, S.A.·Product code MRM·January 8, 2004

    METAL CUTTING WH-2

    FDA Adverse Event
    Malfunction ·MEDTRONIC MIDAS REX·Product code HBE·April 18, 2003

    GYNECARE GYNEMSH PS 4INX6IN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTO·November 9, 2022

    TRAPEASE PERMANENT VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code DTK·October 18, 2005

    ONE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·August 20, 2003

    ENDOTAK C

    FDA Adverse Event
    Death ·CARDIAC PACEMAKERS, INC·Product code LWS·May 7, 2004

    ENDOTAK C

    FDA Adverse Event
    Death ·CARDIAC PACEMAKERS, INC·Product code LWS·May 7, 2004