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

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    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

    GENESIS II TOTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    DCI Edge Dental Chair with Operative Unit

    FDA 510(k)
    FDA Class 1 ·Dental

    FLEXISKIN POLYMER COATED LATEX EXAMINATION GLOVES, POWDER FREE, NON-STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CAPSUREFIX NOVUS

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

    MICRUS MICROCOIL SYSTEM

    FDA Adverse Event
    Injury ·MICRUS ENDOVASCULAR CORPORATION·Product code MJN·December 29, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 23, 2014

    SIMPLE PREP CARBIDE

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