BEUDAMED
    9 results · 20ms · 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

    NEEDLE CASSETTE FOR SPEEDSTICH

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP·Product code GAT·February 22, 2012

    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

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 8, 2013

    BARDEX ALL SILICONE FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·PRODUCTOS PARA EL CUIDADO DE LA SALUD·Product code EZL·February 24, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·November 12, 2010

    SIMPLE PREP CARBIDE

    FDA Adverse Event
    Injury ·COLTENE WHALEDENT INC.·Product code EJL·February 3, 2022