BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    MONOJECT SICKLE CELL KIT

    FDA 510(k)
    FDA Class 2 ·Hematology

    HYDROMASSAGE EQUIP. MODEL 1000

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·April 28, 2016

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 14, 2014

    DOVER

    FDA Adverse Event
    COVIDIEN·Product code FCE·September 25, 2012

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·August 3, 2010

    NEURO SPG-1X1"-STERILE- 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·February 20, 2025

    NEURO SPNG-1/2X3"-STRL- 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

    NEURO-SP-1/2X1/2"-STRL 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

    NEURO-SP-1/2X1/2"-STRL 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

    NEURO-SP-1/2X1/2"-STRL 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·February 7, 2025