BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    Ekso™ (version 1.1) and Ekso GT™ (version 1.2)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CAPNOSTREAM20P WITH HIFI C02 MONITORING

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GE LOGIQ I, LOGIQ E AND VIVID E

    FDA 510(k)
    FDA Class 2 ·Radiology

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 3, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 29, 2011

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·August 29, 2008

    INTIMA II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·October 31, 2018

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 4/10MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 4, 2019

    ALINITY HQ ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code GKZ·December 22, 2025