BEUDAMED
    22 results · 23ms · Sources: EU EUDAMED, US FDA

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    PRECISION RXI ANALOG X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDGEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    EMIT 2000 QUINIDINE ASSAY, MODEL OSR4Q229

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    9616026-2006-00240

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616026-2006-00244

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    9616026-2006-00239

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    9616026-2006-00222

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    9616026-2006-00252

    FDA Adverse Event
    Other ·Product code FII·June 21, 2006

    9616026-2006-00245

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    9616026-2006-00253

    FDA Adverse Event
    Other ·Product code FII·June 21, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    9616026-2006-00221

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    PRISMAFLEX SETS (M)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·May 13, 2024

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·April 8, 2013

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·April 6, 2011

    ENDOTAK ENDURANCE EZ

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

    PRISMAFLEX SETS (M & ST)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·March 28, 2023