BEUDAMED
    6 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    1282497-2001-00002

    FDA Adverse Event
    Injury ·KENDALL CORP·Product code KNT·February 1, 2001

    SOFTCLIX ® LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·March 26, 2013

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·March 11, 2011

    SPIDERFX EMBOLIC PROTECTION DEVICE

    FDA Adverse Event
    Injury ·EV3 INC.·Product code NTE·March 27, 2008

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·February 23, 2024

    PRINEO SKIN CLOSURE SYSTEM UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OMD·February 23, 2024