BEUDAMED
    6 results · 22ms · 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 ×

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KWA·June 4, 2014

    PRSVN ALLPOLY TIB RMLL SZ4 7MM

    FDA Adverse Event
    Injury ·DEPUY RAYNHAM·Product code HRY·November 29, 2012

    EXCELCARE BARIATRIC BED FRAME

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC·Product code FNL·September 28, 2010

    OXYSEPT

    FDA Adverse Event
    Injury ·AMO(HANGZHOU) CO., LTD.·Product code LPN·June 5, 2023

    CONSEPT 1 STEP LL

    FDA Adverse Event
    Injury ·AMO(HANGZHOU) CO., LTD.·Product code LPN·August 28, 2023

    EXABLATE 4000

    FDA Adverse Event
    Injury ·INSIGHTEC, LTD.·Product code POH·August 29, 2017