BEUDAMED
    15 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·December 7, 2010

    G7 SCREW 6.5MM X 30MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·November 10, 2017

    BONE SCREW SELF-TAPPING 25 MM LENGTH 6.5 MM DIA.

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·November 13, 2017

    BONE SCREW SELF-TAPPING 35 MM LENGTH 6.5 MM DIA.

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·September 22, 2017

    BONE SCREW SELF-TAPPING 25 MM LENGTH 6.5 MM DIA.

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·September 22, 2017

    BONE SCREW SELF-TAPPING 30 MM LENGTH 6.5 MM DIA.

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·September 22, 2017

    BONE SCREW SELF-TAPPING 35 MM LENGTH 6.5 MM DIA.

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·September 22, 2017

    G7 ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·September 6, 2017

    G7 ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·September 6, 2017

    G7 ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·.·Product code JDI·September 6, 2017

    G7 OSSEOTI MULTIHOLE 56MM F

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 21, 2017

    G7 ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·September 6, 2017

    G7 DUAL MOBILITY SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWY·September 6, 2017

    G7 DUAL MOBILITY SYSTEM, ACTIVE ARTICULATION SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWY·September 6, 2017

    G7 ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·September 6, 2017