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

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    HARMAC BALLOON WEDGE PRESSURE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295246251·SIGMA TC3 RP INSERT TRIAL SIZE 2.5 20mm

    6MP Color LCD Monitor, RadiForce RX660, RX660-AR

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYSTEMATE URIC ACID (URCA) ITEM NUMBER 65422

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    FX OXY W/HR & ART FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORP·Product code DTZ·May 30, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·February 15, 2013

    COURIER GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BRIVANT LTD·Product code DQX·December 15, 2010

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 6, 2017