BEUDAMED
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    COCCIDIOIDES IMMITIS, ANTISERUM POS.

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ZEPHIR® Anterior Cervical System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00681490540957·SCREW 8792717 VASD CNCLLS 4.0X17MM

    DIRECT DIGITIZER, REGIUS MODEL 210

    FDA 510(k)
    FDA Class 2 ·Radiology

    da Vinci SP Surgical System

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

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 2, 2014

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 16, 2012

    ENPULSE

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·August 11, 2010

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026