BEUDAMED
    33 results · 28ms · Sources: EU EUDAMED, US FDA

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    NON-STERILE, POWDER FREE BLACK NITRILE EXAMINATION GLOVES WITH CHERRY FLAVOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NEUROEDGE INFUSION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACTIVA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code MHY·May 18, 2012

    HAHN TAPERED IMPLANT Ø3.0 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 2, 2024

    HAHN TAPERED IMPLANT Ø3.0 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·March 25, 2024

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MRU·January 27, 2015

    SOLETRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code MHY·May 18, 2012

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·May 12, 2015

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·September 16, 2013

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·May 8, 2015

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·September 16, 2013

    ELECTRONIC GAS BLENDER

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·October 19, 2015

    STOCKERT S3 GAS BLENDER

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014

    MERIT CUSTOM KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DRS·May 3, 2013

    AQUIFY MPS

    FDA Adverse Event
    Injury ·CIBA VISION CANADA, INC.·Product code LPN·August 27, 2014

    8800

    FDA Adverse Event
    Malfunction ·GE MED SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·May 11, 2011

    S3 GAS BLENDER SYSTEM

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017

    S3 GAS BLENDER SYSTEM

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017