BEUDAMED
    455 results · 47ms · Sources: EU EUDAMED, US FDA

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    PLUS ORTHOPEDICS CEMENTED HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TC-PLUS SB SOLUTION

    FDA Adverse Event
    Other ·PLUS ORTHOPEDICS AG·Product code JWH·January 14, 2005

    9612771-2006-00021

    FDA Adverse Event
    Injury ·Product code KWB·September 1, 2006

    9612771-2007-00001

    FDA Adverse Event
    Injury ·Product code JWH·January 9, 2007

    TC-PLUS SOLUTION

    FDA Adverse Event
    Injury ·PLUS ORTHOPEDICS AG·Product code JWH·April 26, 2007

    9612771-2006-00022

    FDA Adverse Event
    Injury ·Product code KWB·September 1, 2006

    9612771-2006-00023

    FDA Adverse Event
    Injury ·Product code KWY·September 1, 2006

    NI

    FDA Adverse Event
    Other ·PLUS ORTHOPEDICS AG·Product code ---·November 1, 2005

    TC-PLUS SOLUTION

    FDA Adverse Event
    Injury ·PLUS ORTHOPEDICS AG·Product code JWH·November 8, 2007

    9612771-2006-00030

    FDA Adverse Event
    Injury ·Product code KWR·October 6, 2006

    9612771-2006-00025

    FDA Adverse Event
    Injury ·Product code KWB·September 1, 2006

    9612771-2006-00024

    FDA Adverse Event
    Injury ·Product code KWB·September 1, 2006

    PIGALILEO CAS/NAV TKR SYSTEM

    FDA Adverse Event
    Other ·PLUS ORTHOPEDICS AG·Product code HAW·February 28, 2007

    PIGALILEO CAS/NAV TKR SYSTEM

    FDA Adverse Event
    Other ·PLUS ORTHOPEDICS AG·Product code HAW·February 28, 2007

    PLUS-FIT ACETABULAR CUP

    FDA Adverse Event
    Injury ·PLUS ORTHOPEDICS AG·Product code LZO·November 8, 2007

    MODULAR-PLUS REVISION STEM

    FDA Adverse Event
    Injury ·PLUS ORTHOPEDICS AG·Product code JDI·November 8, 2007

    BIPOLAR PROSTHESIS

    FDA Adverse Event
    Injury ·PLUS ORTHOPEDICS AG·Product code KWY·November 8, 2007

    BOFOR

    FDA Adverse Event
    Injury ·PLUS ORTHOPEDICS AG·Product code LZO·November 8, 2007

    *

    FDA Adverse Event
    Injury ·PLUS ORTHOPEDICS AG·Product code ---·June 6, 2007

    BICON-PLUS ACETABULAR COMPONENTS

    FDA Adverse Event
    Injury ·PLUS ORTHOPEDICS AG·Product code LPH·May 24, 2007