BEUDAMED
    3,114 results · 23ms · Sources: EU EUDAMED, US FDA

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    TRACLUX

    FDA UDI
    SUNOPTIC TECHNOLOGIES LLC·M678HHR0·TracLux HandLite Retractor Components include t...

    NA

    FDA UDI
    ST. JUDE MEDICAL, INC.·05415067009753·Rigid Holder Handle

    QUANTICEL HHR # L500 AND L501

    FDA 510(k)
    FDA Class 2 ·Hematology

    QUANTICEL HHR, L531 AND L532

    FDA 510(k)
    FDA Class 2 ·Hematology

    QUANTICEL HHR TWO HUMAN HEMATOLOGY REFERENCE

    FDA 510(k)
    FDA Class 2 ·Hematology

    Biodesign Additae

    FDA UDI
    COOK BIOTECH INCORPORATED·00827002592872·Biodesign Additae Hiatal Hernia Graft

    QUANTICEL HHR + TWO HUMAN HEMATOLOGY W/PLATELETS

    FDA 510(k)
    FDA Class 2 ·Hematology

    ESOPHYX Z+

    FDA Adverse Event
    Injury ·ENDOGASTRIC SOLUTIONS, INC·Product code ODE·October 6, 2023

    UNKNOWN COPELAND SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·May 26, 2016

    Biodesign Additae

    FDA UDI
    COOK BIOTECH INCORPORATED·00827002515796·Biodesign Additae Hiatal Hernia Graft

    UNKNOWN COPELAND SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·May 26, 2016

    UNKNOWN COPELAND SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·May 26, 2016

    UNKNOWN COPELAND SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·May 26, 2016

    UNKNOWN COPELAND SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·May 26, 2016

    UNKNOWN COPELAND SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·May 26, 2016

    UNKNOWN COPELAND SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HSD·May 26, 2016

    ESOPHYX Z+

    FDA Adverse Event
    Injury ·ENDOGASTRIC SOLUTIONS, INC·Product code ODE·March 16, 2024

    ESOPHYX Z+

    FDA Adverse Event
    Injury ·ENDOGASTRIC SOLUTIONS, INC·Product code ODE·June 28, 2024

    ESOPHYX Z+

    FDA Adverse Event
    Injury ·ENDOGASTRIC SOLUTIONS, INC·Product code ODE·March 16, 2024

    1.5T LINX, 17 BEADS

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·November 11, 2019