BEUDAMED
    14 results · 20ms · Sources: EU EUDAMED, US FDA

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    RADIAL IMMUNO-TEST FOR HUMAN FACTOR B

    FDA 510(k)
    FDA Class 2 ·Immunology

    HEINE MINI 3000(R) OPHTHALMOSCOPE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    STRYKER PLATING SYSTEM PERIARTICULAR PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RECEPTAL CANISTER 1000 ML CE

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD.·Product code GCX·May 25, 2012

    RECEPTAL 1.5LITER PE/CE WITH (50/CASE)

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code GCX·August 1, 2011

    NON-PVC RECEPT LINER 2000ML/CE(50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code GCX·June 21, 2011

    NON-PVC RECEPT. LINER 2000ML/CE(50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code GCX·June 21, 2011

    NON-PVC RECEPT LINER 2000ML/CE(50/CS)

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code GCX·June 21, 2011

    RECEPTAL 1.5 LITER PE/CE WITH (50/CASE)

    FDA Adverse Event
    Injury ·HOSPIRA LTD.·Product code GCX·November 18, 2010

    RECEPTAL 1 LITER/CE WITH VALVE (50/CAS)

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code GCX·June 24, 2011

    RECEPTAL 1 LITER/CE WITH VALVE (50/CAS)

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code GCX·June 24, 2011

    CORAIL2 ANTERIOR BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·May 27, 2014

    FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·November 14, 2012

    GORE HEMOBAHN ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES·Product code NIO·September 8, 2010