BEUDAMED
    29 results · 23ms · Sources: EU EUDAMED, US FDA

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    Nitrile Powder Free Examination Glove with Low Dermatitis Potential Claim and Tested for Use with Chemotherapy Drugs (Blue)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694027311·2.4mm X 42mm Cannulated Headless Screw

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613102333·Clear Cornea UniBevel Double Bevel Knife, Angle...

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613102340·2.4mm Clear Cornea UniBevel Double Bevel Knife ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694069106·Cannulated 2.4 x 42mm Headless Screw Sterile Qty 5

    E.S.O. (ELECTRO SENSOR OXI)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RADIAL-EMITTING SHAPED FIBER OPTIC DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    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 18, 2024

    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

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code NVY·January 13, 2014

    UNKNOWN DEPUY TIBIAL STEM

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 17, 2013