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

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    Litho 60; Litho 100; Litho 150

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694023238·FPS 3.5/4.0mm 8mm Step Plate

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122315·KWire .094 x 9" (2.4x225mm)

    MORELAND

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295123293·MORELAND REV INST TREPHINE REAMER 11mm 5.5 IN

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517110791·

    BD NEXIVA SINGLE PORT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·January 30, 2025

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694077989·FPS 3.5/4.0 8mm Step Plate Sterile Qty 2

    BAYER ADVIA 2120 HEMATOLOGY ANALYZER WITH AUTOSLIDE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    AVS AS PEEK Spacer

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SOL 8.0 FULL PC 12/14

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·September 16, 1999

    HEMOSPHERE ALTA

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code QAQ·November 18, 2025

    HEMOSPHERE ALTA

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code QAQ·August 20, 2025

    MATRIX2 STANDARD 360 SR COIL

    FDA Adverse Event
    Injury ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORPORATION·Product code HCG·November 19, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    HUDON RCI/SHERIDAN

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·July 16, 2013

    HEMOSPHERE ALTA

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code QAQ·November 18, 2025

    HEMOSPHERE ALTA

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code QAQ·November 18, 2025

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·August 22, 2007

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 7, 2020

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 7, 2020