BEUDAMED
    524 results · 31ms · Sources: EU EUDAMED, US FDA

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    HU-FRIEDY

    FDA UDI
    HU-FRIEDY MFG. CO., LLC·10889950079536·LIGATURE DIRECTORS- DR. KNIGHT HANDEL#6

    GENESIS II

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. ORTHOPAEDIC DIVISION·Product code JWH·May 9, 2011

    INTERVERTEBRAL FUSION DEVICE W/INTEGRATED FIXATION,CERVICAL

    FDA Adverse Event
    Injury ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code OVE·January 16, 2018

    KNEE-DUMMY IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·January 17, 2019

    KNEE-DUMMY IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·January 10, 2019

    KNEE-DUMMY IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·January 17, 2019

    KNEE-DUMMY IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·January 17, 2019

    TRANSFORM

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LDK·April 10, 2018

    KNEE-DUMMY IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 23, 2019

    KNEE-DUMMY IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 23, 2019

    KNEE-DUMMY IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 23, 2019

    KNEE-DUMMY IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 23, 2019

    UNKN GENESIS II TOTAL KNEE FEM COMP COCR CEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HRY·June 13, 2022

    UNKN GENESIS II TOTAL KNEE TIB INSERT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HRY·June 11, 2022

    ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·September 10, 2015

    ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·September 10, 2015

    ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code NKB·September 10, 2015

    ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·September 10, 2015

    ORTHOSIS, PEDICLE SPINAL FIXATION, FOR DDD

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code NKB·September 10, 2015

    Device, Sensing, Optical Contour

    FDA classification
    FDA Unclassified ·Device, Sensing, Optical Contour