BEUDAMED
    5 results · 24ms · 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 Status: Malfunction ×

    K083526

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·May 7, 2018

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 20, 2021

    ACCU-CHEK ® AVIVA COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·June 19, 2014

    PURELIGHT

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC·Product code DQA·October 19, 2010

    SWAN-GANZ BIPOLAR PACING CATHETER FOR FEMORAL INSERTION

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code LDF·December 21, 2012