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

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    SMARTFLOW CATHETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    FOERSTER SPONGE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896021587·FOERSTER SPONGE FORCEPS STRAIGHT SMOOTH JAW

    PKS BILL

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PERMACOL SURGICAL IMPLANT

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

    BD INSYTE AUTOGUARD WINGED

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 30, 2024

    Shaver System

    FDA UDI
    STRYKER CORPORATION·00857326005772·Shaver Blade 3mm Single Use Double Serrated 60 ...

    PERMACOL 10X15 1.5MM

    FDA Adverse Event
    Death ·COVIDIEN, FORMERLY TISSUE SCIENCE LABORATORIES, PLC·Product code FTL·September 3, 2013

    BD INSYTE AUTOGUARD WINGED

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 10, 2024

    BD INSYTE AUTOGUARD WINGED

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 10, 2024

    ALIGN® TO URETHRAL SUPPORT SYSTEM - HOOK + HALO

    FDA Adverse Event
    Injury ·BARD SHANNON LIMITED·Product code OTN·May 17, 2013

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·June 10, 2011

    VERSACARE

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

    Depuy P.F.C. E knee system, all polyethylene curved tibial component, Sz 2, 10 mm; Ref 96-0621.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005