BEUDAMED
    28 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ERBEFLO Olympus Scope Port Connector

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528127940·2.4 X 44mm Cannulated Headed Screw, T7

    POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·October 17, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 9, 2018

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·January 11, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 14, 2025

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·January 21, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·December 21, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 11, 2013

    KRH BUSHING STANDARD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·July 19, 2011

    UNICEL DXC 800 PRO SYNCHRON CHEMISTRY ANALYZER

    FDA Adverse Event
    Other ·BECKMAN COULTER, INC.·Product code JJE·September 12, 2008

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 3, 2018