BEUDAMED
    11 results · 27ms · 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 ×

    PLATE CDC ANAEROBE 5% SB 100 EA JP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·September 9, 2021

    COBAS C 503 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 16, 2024

    COBAS C 503 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 8, 2024

    COBAS C 503 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 6, 2024

    PLATE CDC ANAEROBE 5% SB 20 EA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JSG·June 28, 2021

    SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 9, 2014

    GORE VIABIL BILIARY ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code FGE·October 16, 2012

    EZLIFT

    FDA Adverse Event
    Injury ·EZ WAY, INC.·Product code FNG·August 10, 2010

    COBAS C 303 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·July 22, 2024

    COBAS C 503 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 31, 2024

    PLATE CDC ANAEROBE AGAR 5% SB 90MM 20

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSG·February 17, 2022