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

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    CHRONO-LOG WHOLE BLOOD AGGREGOMETER (WBA) 591/592

    FDA 510(k)
    FDA Class 2 ·Hematology

    StarGuide MDD to MDR Upgrade

    FDA UDI
    G E MEDICAL SYSTEMS ISRAEL LTD.·00195278870490·StarGuide SW and Labels Upgrade

    DEPUY PINNACLE METAL-ON-METAL ACETABULAR CUP LINERS

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    nva, nvp, and nvt

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REF H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·August 9, 2016

    PFR KIT ¿ UPHOLD LITE VAGINAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 14, 2013

    UNK DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 7, 2011

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014