BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    ADVIA Centaur® Digoxin assay

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Reveal

    FDA UDI
    Oticon A/S·05707131341365·G20, BTE 13 PP 2.4G 105 C091 REVEAL

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·February 11, 2014

    ACCUVIX XG DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRAXCESS 14EX GUIDEWIRE AND TRAXCESS DOCKING WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·August 16, 2012

    AFFINITY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code HDD·October 7, 2008

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 27, 2013

    MCA MED APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDO·August 5, 2011

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·November 6, 2014

    MIRU 1DAY UPSIDE (MIDAFILCON A)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·January 22, 2025