BEUDAMED
    14 results · 30ms · Sources: EU EUDAMED, US FDA

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    VACVENT

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    ALILITE HEEL PADS

    FDA UDI
    ALIMED, INC.·00733657239904·

    I-STAT CARDIAC MARKERS CONTROL LEVEL 1, 2, AND 3; CARDIAC MARKERS CALIBRATION VERIFICATION CONTROL SET

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NDOHD HIGH DEFINITION IMAGING SYSTEM (NDOHD)

    FDA 510(k)
    FDA Class 2 ·Radiology

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 7, 2014

    BD ALARIS¿ SMARTSITE¿ GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·February 9, 2023

    EVOLVE(R)

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWI·October 3, 2018

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 28, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·December 10, 2010

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·July 14, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 7, 2014

    BD GEM V/NV 20D 0.2 FLTR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·July 28, 2022

    GEM V/NV NTG 20DP 20PK

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 10, 2020

    BD ALARIS¿ SMARTSITE¿ GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·January 20, 2023