BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    ECOM ENDOTRACHEAL CARDIAC OUTPUT MONITOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Oticon

    FDA UDI
    Oticon A/S·05707131256102·NERA PRO, BTE 13 WL 85 CNB

    ArgenZ HT+ 98x30 ML OM2B

    FDA UDI
    ARGEN CORPORATION, THE·D818131765·Dental porcelain/ceramic restoration kit

    KYPHON ANCHOR FACET SCREW SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    FULL CORE BIOPSY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ALARIS® PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·November 12, 2018

    PINNACLE 300 ACET CUP 58MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·May 29, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 16, 2011

    CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code LWR·August 21, 2008