BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    HEARTPORT DIRECT AORTIC RETURN CANNULA WITH INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VSP (VARIABLE SCREW PLACEMENT)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RICH-MAR HV-2000 ELECTRICAL MUSCLE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PROFILE BIABUT 4.0 -Ø5.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·February 24, 2026

    NV GXL LINR, NTRL, 36MM ID, GROUP 3 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code LZO·March 15, 2024

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·January 18, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·August 4, 2014