BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    KSEA MODEL 383320 20 ANGIOMAT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNCHRON URIC ACID

    FDA Adverse Event
    BECKMAN COULTER INC.·Product code KNK·June 10, 2011

    HEMASTAIN WRIGHT STAIN

    FDA 510(k)

    CYCLONE, MODEL MAICAM 180

    FDA 510(k)
    FDA Class 2 ·Radiology

    GORE VIABAHN ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·April 20, 2010

    CARPENTIER-EDWARDS PERIMOUNT THEON PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·August 3, 2015

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 9, 2014

    M2A 38MM ONE-PIECE CUP 38MM X 56 OD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 13, 2011