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

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    CurrentBody Skin RF

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NA

    FDA UDI
    Medos International Sàrl·10886705011360·FULLY FLUTED REAMER, STERILE 40 - 130mm (Plus o...

    METRIXCARE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LOTUS

    FDA 510(k)
    FDA Unclassified ·Unknown

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·August 26, 2011

    HARMONY IQ CUSTOM INTEGRATION SYSTEM

    FDA Adverse Event
    VTS MEDICAL SYSTEMS·Product code LMD·November 6, 2014

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·July 18, 2013

    DXTEND HIGHMO PE CUP D38 +3MM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code PHX·July 9, 2025

    RS GLENOID PLATE R POST AUG, 8 DEG, RIGHT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·April 30, 2024

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 9, 2026

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 10, 2026

    BD VERITOR¿ PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code PSZ·March 7, 2025