BEUDAMED
    13 results · 41ms · Sources: EU EUDAMED, US FDA

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    PRESSURE MANIFOLD, MODEL BC 110

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Myo/Wire II

    FDA UDI
    A & E MEDICAL CORPORATION·10841291101741·SS Suture, 8 per sleeve

    FIXATION STYLETS, MODELS 335-287 AND 335-288

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DISPOSABLE STORAGE CAP

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·March 23, 2022

    CADD MEDICATION CASSETTE

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·July 14, 2022

    CADD

    FDA Adverse Event
    Malfunction ·NULL·Product code FPA·August 17, 2021

    CADD MEDICATION CASSETTES

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·June 6, 2022

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·ASPEN SURGICAL PRODUCTS·Product code FZZ·March 12, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 15, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 7, 2008

    6.5MM TI RECON SCREW WITH T25 STARDRIVE 95MM

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·April 23, 2018

    6.5MM TI RECON SCREW WITH T25 STARDRIVE 105MM

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·April 23, 2018