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

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    AE-105D DIAGNOSTIC TYMPANOMETER

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Stimuplex®

    FDA UDI
    B. BRAUN MEDICAL INC.·04022495101211·Stimuplex® A, 30° bevel (4894260)

    MODEL 476-03 PACING LEAD

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    RECON-2 FLOW CONTROLLER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    NA

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code NMJ·February 19, 2014

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·November 3, 2010

    COOK CELECT NAVALIGN FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·December 27, 2012

    Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260

    FDA Recall
    Open, Classified ·B Braun Medical Inc·Product code BXN·May 17, 2024

    Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260

    FDA Enforcement
    Class II ·Ongoing·B Braun Medical Inc·June 19, 2024