BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    POLARIS SPINAL SYSTEM - BALLISTA II RODS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    NON-MYDRIATIC AUTO FUNDUS CAMERA AFC-330 WITH IMAGE FILING SOFTWARE NA VIS-EX

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    8MP COLOR LCD MONITOR, REDIFORCE RX840

    FDA 510(k)
    FDA Class 2 ·Radiology

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 26, 2014

    WALLFLEX BILIARY RX FULLY-COVERED STENT SYSTEM, MODEL M00570500,M00570510, M0057

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·June 14, 2011

    OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LLC·Product code LPN·May 17, 2024

    OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LLC·Product code LPN·May 17, 2024

    BAIR HUGGER / 3M

    FDA Adverse Event
    Injury ·3M·Product code DWJ·November 23, 2016