BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    HelixAR Electrosurgical Generator with Argon Beam Coagulation, HelixAR Mobile Pedestal

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

    STERILCONTAINER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYNGO RT THERAPIST CONNECT WORKSPACE, V4.2

    FDA 510(k)
    FDA Class 2 ·Radiology

    ROUND FILTER POLYPROVPYLENE

    FDA Adverse Event
    Malfunction ·SPS MEDICAL SUPPLY CORP·Product code FRG·June 25, 2013

    PROXIMATE** RELOADABLE LINEAR CUTTER WITH SAFTEY LOCK-OUT

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 17, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 20, 2011

    COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE LTD.·Product code FRN·September 19, 2008

    PINNACLE SECTOR II CUP 54MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 24, 2019