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

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    ALARIS SMARTSITE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FPA·January 26, 2026

    BD Alaris™ Pump Infusion Sets

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DIOLASE 10S

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

    ORTHOPILOT HTO MODULE

    FDA 510(k)
    FDA Class 2 ·Neurology

    CAPTURE-R READY-ID

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·March 25, 2015

    ASR XL SLV ADAP 12/14 +8

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code JDI·August 4, 2017

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·November 3, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 24, 2011

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·July 11, 2013

    ECHO

    FDA Adverse Event
    Malfunction ·IMMUCOR·Product code KSZ·March 16, 2009