BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LGN PS HIGH FLEX XLPE SZ 1-2 13MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017

    GII PS HI FLEX ISRT SZ 7-8 9

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·July 19, 2017

    LGN PS HIGH FLEX XLPE SZ 1-2 13MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017

    GII ARTICULAR INSERTER/EXTRACT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBH·February 9, 2018

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 9, 2013

    TPE SET, SPECTRA

    FDA Adverse Event
    Injury ·CARIDIANBCT·Product code LKN·December 29, 2010

    ECHELON LINEAR CUTTER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 23, 2014

    CRTS RA VLV ONLY

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·October 10, 2023