BEUDAMED
    21 results · 25ms · Sources: EU EUDAMED, US FDA

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    ROSA Knee System

    FDA 510(k)
    FDA Class 2 ·Neurology

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·February 1, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·February 4, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·February 1, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·April 4, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·March 9, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Malfunction ·ZIMMER CAS·Product code OLO·March 21, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code OLO·November 8, 2021

    ROSA KNEE PLATFORM GB PL G

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·January 13, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·January 10, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·April 6, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·January 10, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·May 6, 2022

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Malfunction ·ZIMMER CAS·Product code OLO·November 15, 2021

    ROSA RECON PLATFORM 220V

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·November 11, 2021

    FIX PIN FLTD 3.2DX150MM 2 PACK

    FDA Adverse Event
    Injury ·ZIMMER CAS·Product code OLO·March 24, 2025

    EU-TTG IGA AND EU-TTG IGG

    FDA 510(k)
    FDA Class 2 ·Immunology

    PRISM ACQUIRE (VERSION 1.5), PRISM PROCESS (VERSION 1.5), PRISM VIEW (VERSION 2.5)

    FDA 510(k)
    FDA Class 2 ·Radiology

    POLARIS DX¿ STEERABLE DIAGNOSTIC CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SAN JOSE·Product code DRF·July 28, 2011

    M2A-MAGNUM MOD HD SZ 42MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 21, 2013