BEUDAMED
    8 results · 28ms · 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 ×

    RMI ARTERIAL PERFUSION CANNULA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ES 22

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    TOTAL BILIRUBIN FOR DEMAND ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    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

    PRODISC-C IMPLANT MEDIUM DEEP 5MM-STERILE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MJO·June 20, 2019

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 25, 2014

    LTV

    FDA Adverse Event
    Malfunction ·CAREFUSION 203, INC.·Product code CBK·November 3, 2010

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·November 15, 2012