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

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    SULZER MEDICA

    FDA Adverse Event
    Injury ·SULZER MEDICA·Product code KWB·January 17, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Malfunction ·SULZER ORTHOPEDICS (DIV. SULZER MEDICA)·Product code KWB·January 29, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Malfunction ·SULZER ORTHOPEDICS (DIV SULZER MEDICA)·Product code KWB·January 29, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Malfunction ·SULZER ORTHOPEDICS (DIV. SULZER MEDICA)·Product code KWB·January 29, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Malfunction ·SULZER ORTHOPEDICS (DIV. SULZER MEDICA)·Product code KWB·January 29, 2001

    SULZER MEDICA

    FDA Adverse Event
    Malfunction ·*·Product code KWY·July 20, 2001

    INTER-OP ACETABULAR SYSTEM

    FDA Adverse Event
    Malfunction ·SULZER MEDICA·Product code LPH·June 12, 2001

    SULZERMEDICA

    FDA Adverse Event
    Injury ·ZIMMER·Product code HSH·October 27, 2005

    SULZERMEDICA

    FDA Adverse Event
    Injury ·SULZER MEDICA, SULZER ORTHOPEDICS, INC.·Product code LPH·May 3, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·March 20, 2001

    SULZER MEDICA

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS·Product code JDI·March 19, 2003

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·April 18, 2001

    ZIRCONIA HD +4MM NK 28MM

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS, INC.·Product code LZO·April 15, 2003

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER MEDICA, SULZER ORTHOPEDICS, INC.·Product code KWB·February 26, 2001

    HEMI POR SHL W/SEALED SCWHLS SZ55MM I-O

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code LPH·April 20, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER MEDICA, SULZER ORTHOPEDICS INC.·Product code KWB·February 26, 2001

    INTER-OP ACETABULAR SHELL

    FDA Adverse Event
    Injury ·SULZER MEDICA, SULZER ORTHOPEDICS, INC.·Product code KWB·January 3, 2001

    HEMI POR SHL W/SEALED SCWHLS SZ59MM I-O

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code LPH·April 20, 2001

    SULZER MEDICA

    FDA Adverse Event
    Injury ·SULZER MEDICA SULZER ORTHOPEDICS INC·Product code KWB·February 14, 2001

    SULZER MEDICA

    FDA Adverse Event
    Injury ·SULZER MEDICA SULZER ORTHOPEDICS INC.·Product code KWB·February 14, 2001