BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909135952·REVELATION DIAMOND 878K-012C - 5 PACK

    Indigo Aspiration System - Aspiration Catheter 7 and Separator 7

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PREMIER III PHASED ARRAY CTL SPINE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 12, 2010

    ADVIA CENTAUR XP TROPONIN ULTRA (TNI ULTRA) ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·July 3, 2014

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON- IRVINE TECHNOLOGY CENTER·Product code HQC·December 21, 2012

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·December 10, 2024

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·January 5, 2023