BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    DSL ACTIVE AFP ELISA, MODEL DSL-10-8400

    FDA 510(k)
    FDA Class 2 ·Immunology

    Eargo 5

    FDA UDI
    Eargo, Inc.·00850010429311·Medium Closed Petals

    MAGNETOM Aera

    FDA 510(k)
    FDA Class 2 ·Radiology

    MOBILECARE MONITOR, MODEL 2100

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ROTATING HEMOSTATIC VALVE

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DYB·March 5, 2013

    CAPSURE Z NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 7, 2014

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·June 9, 2021

    ZIMMON PANCREATIC STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 16, 2020