BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Universal Spike

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Oticon

    FDA UDI
    Oticon A/S·05707131280572·H16V2, BTE 13 WL 85 STG

    REZUM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·April 23, 2024

    RENASYS F/-AB ABDOMINAL WOUND DRESSING KIT

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

    TRIPORE TDD (HA), TRIPORE TDD (BP90), TRIPORE TDD (BP15)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    X-SUIT NIR COVERED BILIARY METALLIC STENT

    FDA Adverse Event
    Malfunction ·MEDINOL LTD.·Product code FGE·December 27, 2017

    AML LG STATURE 13.5MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. - 1818910·Product code LPH·June 6, 2013

    EON MINI IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 21, 2011

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008

    ARTOURA BREAST TISSUE EXPANDER

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·August 21, 2023