BEUDAMED
    6 results · 19ms · 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

    PLATE CDC ANAEROBE 5% SB 20 EA

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

    PLATE CDC ANAEROBE AGAR 5% SB 90MM 20

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

    ECHELON LINEAR CUTTER RELOAD

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 9, 2014

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Injury ·CAREFUSION CORP·Product code FPA·October 17, 2012

    ELECSYS 2010 RACK

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS CORPORATION·Product code MMI·August 17, 2010