BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    K-Pack II Needle-21G x 2

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486018429·HIP ACETABULAR INSTRUMENT KIT PULL-OUT UPPER TRAY

    Oticon

    FDA UDI
    Oticon A/S·05707131286604·RIA2, MINIRITE 312 WL SIL

    IRIS Anterior Cervical Plate System

    FDA UDI
    Life Spine, Inc.·00190837060831·Iris Cervical Screw Driver

    Femoral Trial Size 1

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215073626·

    ELITECH CLINICAL SYSTEMS PHOSPHORUS, URIC ACID MONO SL AND UREA UV SL REAGENTS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MILLENNIUM SERIES, INCLUDING MILLENNIUM B, B+, B2 AND BU

    FDA 510(k)
    FDA Class 2 ·General Hospital

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·February 27, 2023

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 6, 2013

    PINNACLE PELVIC FLOOR REPAIR KIT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FTM·September 3, 2008

    CRE FIXED WIRE BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNQ·August 21, 2008