BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    Genesis II XLPE Resurfacing Patellar Components

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Oticon

    FDA UDI
    Oticon A/S·05707131286161·H16V2 TI, RITE 312 WL CNB

    MAKOPLASTY

    FDA UDI
    MAKO SURGICAL CORP.·00848486018382·HIP POWER EQUIPMENT KIT LOWER TRAY

    Vilex Guidewire

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731120588·Guidewire 2.4x150mm Sgl Trocar

    FERGUSON GALLSTONE SCOOP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896024212·FERGUSON GALLSTONE SCOOP MEDIUM DOUBLE ENDED OV...

    AOS HUMERAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CONTIPLEX D CONTINUOUS NERVE BLOCK SET, MODEL 331687, 331686, 331685, 331680

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 25, 2024

    SPECTRANETICS QUICK-CROSS SUPPORT CATHETER

    FDA Adverse Event
    Injury ·THE SPECTRANETICS CORPORATION·Product code DQY·March 6, 2019

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 1, 2015

    600CMS IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 29, 2013

    TEMP PUMP TEMPERATURE

    FDA Adverse Event
    Malfunction ·STRYKER CORP. DBA GAYMAR·Product code ILO·June 10, 2011

    SYNERGY VERSITREL

    FDA Adverse Event
    Injury ·MEDTRONIC SWISS MANUFACTURING FACILITY·Product code LGW·September 3, 2008

    MEDTRONIC DUAL CHAMBER TEMPORARY EXTERNAL PACEMAKER 510(K) K150246

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DTE·February 10, 2021