BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    MAGNET RETRIEVAL CATHETER

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

    RENEW NEUROSTIMULATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    STRYKER SWITCHPOINT INFINITY 3 CONTROL SYSTEM, MODEL: 067-8001-000

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

    SNAP-RING FOR 52MM OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·December 4, 2007

    STERLING

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·June 5, 2020

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 27, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 17, 2010

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 12, 2012