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

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    IntelliSense Drill

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    REPOL ANGIMESH, ANGIMESH PRE, FOLDED MESH, REPOL PLUG BASIC, REPOL PLUG CAP, REPOL PLUG FLOWER AND WINGS MESH

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

    QUADROX-I PEDIATRIC MICROPOROUS MEMBRANE OXYGENATOR WITH INTEGRATED ARTERIAL FILTER WITH SOFTLINE / BIOLINE COATING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PS FEMORAL COMPONENT CLOSED BOX LGE RIGHT 74 MM CEMENTED

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code JWH·June 3, 2020

    COVIDIEN CATHETERS

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FJS·May 29, 2013

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL ¿ NEUROMODULATION·Product code GZB·September 22, 2014

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·June 28, 2011

    PERF CON TIB BRG LRG 22X60

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020

    NON-POROUS PERF TIB TRAY-LGE

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020

    PERF ANAT TIBIAL STEM 120X14X5

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRR·August 13, 2020

    TRUE METRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·December 30, 2021