BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    BACT/ALERT SV

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ARGENCO 22

    FDA 510(k)
    FDA Class 2 ·Dental

    DAIG PERCUTANEOUS CATHETER INTRO. & REMOVABLE HEMO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FAST-CATH¿ HEMOSTASIS INTRODUCER, CATH-LOCK¿ LOCKING HUB, 12 CM SHEATH, 8.5 F

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code DYB·January 22, 2024

    IMPELLA CP

    FDA Adverse Event
    Injury ·ABIOMED EUROPE GMBH (GERMANY)·Product code KFM·March 4, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·January 14, 2011

    GENTLECATH INTERMITTENT URINARY CATHETER

    FDA Adverse Event
    Malfunction ·UNOMEDICAL S.R.O.·Product code KOD·July 23, 2014