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

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    VERTETRAC

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    FOAM ECG ELECTRODE, 2060 AND 2061

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Performer Guiding Sheath

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IEON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 2, 2012

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 18, 2007

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·December 30, 2013

    PERFORMER MULLINS GUIDING SHEATH

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·January 20, 2023

    PERFORMER MULLINS GUIDING SHEATH

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·January 24, 2024

    PERFORMER INTRODUCER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·November 4, 2022