BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    DTM (DERMATOPHYTE TEST MEDIUM) AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    VuePoint

    FDA UDI
    Nuvasive, Inc.·00887517339201·VuePoint Screw, 4.0x14mm Multi Axial

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690199106·AK3 Congruent Insert Trial Size 4, 14mm

    N/A

    FDA UDI
    SALTER LABS·00607411102738·HIGH FLOW OXYGEN THERAPY KIT THIS KIT CONTAINS:...

    VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EXETER Centralizer, EXETER 2.5mm Plug

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 5, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012

    CAPSURE SP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 10, 2010

    PROPONENT DR SL (Model L201)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025