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

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    RUBY STAR

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

    Oticon

    FDA UDI
    Oticon A/S·05707131283429·H10V2, BTE 13 WL 85 CBE

    BAROSTAT SOFTWARE OPTION

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

    EXPANSE VERTEBRAL BODY REPLACEMENT DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·June 6, 2013

    INOMAX DSIR

    FDA Adverse Event
    Death ·INO THERAPEUTICS LLC/DBA IKARIA·Product code MRN·September 22, 2014

    AUGMENTED INSERT

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·June 29, 2011

    CARTO VIZIGO 8.5F BI-DIRECTIONAL GUIDING SHEATH - MEDIUM

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code DYB·August 31, 2021

    CARTO VIZIGO 8.5F BI-DIRECTIONAL GUIDING SHEATH - MEDIUM

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code DYB·June 8, 2021