BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    EDS3 CLEAR VENT CATH

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·October 19, 2023

    EDS3 CLEAR VENT CATH

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·May 28, 2025

    CODMAN EX. DRAINAGE VENTRICULAR CATH. SET

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC./MEDOS S.A·Product code JXG·October 13, 2005

    EDS3 CLEAR VENT CATH

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·February 21, 2025

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·May 20, 2014

    ALUMINA HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MRA·November 6, 2012

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 25, 2010

    CODMAN EXTERNAL DRAINAGE SYSTEM III

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·February 23, 2016

    EXT DRAINAGE SYSTEM III WITHOUT VENT CATH

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code JXG·May 20, 2014