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

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    SAS SICKLE CELL TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    LUMIX CPS 1 IR Lamp System LUMIX CPS 2 IR Lamp System LUMIX CPS 3 IR Lamp System LUMIX CPS 4 IR Lamp System LUMIX CPS 5 IR Lamp System

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SONICATH ULTRA IMAGING CATHETER, 3.2F,20MHZ MODELS 37410/456221/C1020

    FDA 510(k)
    FDA Class 2 ·Radiology

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·February 14, 2013

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·January 11, 2011

    SCREWDRIVERS

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HXX·July 28, 2014

    UNK - SCREWS: TRAUMA

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·January 28, 2020