BEUDAMED
    8 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 Regulation: Us FDA × Status: Malfunction × Clear all

    SOFTCLIX LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·October 31, 2008

    OSV II

    FDA Adverse Event
    Malfunction ·INTEGRA, BIOT·Product code JXG·August 9, 2011

    BD LUER-LOK¿ 10 ML BULK PACK LUER LOCK TIP WITHOUT SAFETY

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 2, 2022

    IM REAMER, AO FITTING BIXCUT Ø8,0X480 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·April 2, 2014

    IM REAMER, AO FITTING BIXCUT Ø7,5X480 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·April 2, 2014

    IM REAMER, AO FITTING BIXCUT Ø8,0X480 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·April 2, 2014

    IM REAMER, AO FITTING BIXCUT Ø8,5X480 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·April 2, 2014

    BD CATHENA¿ SAFETY IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·July 7, 2022