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

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    Filters Regulation: Us FDA ×

    Venus Velocity Diode Laser System

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

    MODIFICATION TO NUVASIVE NEUROVISION JJB SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    PRONEX

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPECTRA WAVEWRITER?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 8, 2026

    S-ROM M HEAD 36MM +0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 11, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 14, 2011

    ZOLL AUTOPULSE

    FDA Adverse Event
    Malfunction ·ZOLL·Product code DRM·September 16, 2008

    VENATECH CONVERTIBLE

    FDA Adverse Event
    Malfunction ·B.BRAUN MEDICAL SAS·Product code DTK·January 5, 2018