BEUDAMED
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    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    IGG ANTIBODIES TO RUBELLA VIRUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFX·August 12, 2015

    IGG ANTIBODIES TO RUBELLA VIRUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFX·August 3, 2015

    WU'S 4-WHEELED NEO SCOOTER, WT-M3A

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TD-4257 BLOOD GLUCOSE MONITORING SYSTEMS,TD 4257 MULTI BLOOD GLUCOSE MONITORING SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    IGG ANTIBODIES TO RUBELLA VIRUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFX·September 2, 2015

    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

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 17, 2014

    UNKNOWN_ENDOSCOPY_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code NBH·June 21, 2013

    PARADYM

    FDA Adverse Event
    Malfunction ·SORIN BIOMEDICA CRM S.R.L.·Product code NIK·July 28, 2011

    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

    1823260-2015-04057

    FDA Adverse Event
    Malfunction ·September 1, 2015

    ROSA RECON PLATFORM 220V

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