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

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    COBAS INTEGRA LDL DIRECT REAGENT CASSETTE ROCHE CALIBRATOR LDL DIRECT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NUBIC AND RABEA DEVICES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROSA ONE Spine application

    FDA 510(k)
    FDA Class 2 ·Neurology

    CADD LEGACY PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·April 11, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 8, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 23, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 22, 2022

    TOTAL ASR ACET IMP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·February 28, 2013

    VOYAGER RX CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·February 9, 2011

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·July 2, 2014

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 22, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 8, 2022

    CADD LEGACY PLUS PUMPS

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·October 29, 2022

    CADD LEGACY PLUS PUMPS

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·October 24, 2022