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

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    ETEST RIFAMPICIN WITH INDICATIONS FOR S. PNEUMONIAE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    INVOS PM7100 Patient Monitor, INVOS Adult rSO2 Sensor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MULLINS-X, MODEL 250X

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    CRIT-LINE BLOOD CHAMBER

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KOC·June 25, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 31, 2013

    CE INFUSOR LV 5, 12 PACK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 9, 2011

    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

    ASCENT SYSTEM-BEARING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·December 28, 2016

    MORPHEUS CT PICC

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS, INC.·Product code LJS·April 27, 2007