BEUDAMED
    12 results · 25ms · Sources: EU EUDAMED, US FDA

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    HYPODERMIC NEEDLES & STYLETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·20842209121827·

    CORTI-SHURE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TARGET3D FUSION

    FDA 510(k)
    FDA Class 2 ·Radiology

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·LASER WELDING/RHAR,PMMA HAPTICS

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS KR2V, SK21V, S2BV

    DLT TS CER HD 12/14 40MM +1.5

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code LZO·December 29, 2014

    PINNACLE 300 ACET CUP 58MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·December 29, 2014

    ALTRX +4 10D 40IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·December 29, 2014

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·May 30, 2014

    INFUSOMAT SPACE

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·November 15, 2012

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·September 15, 2010