BEUDAMED
    13 results · 18ms · Sources: EU EUDAMED, US FDA

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    E.MEM POWDERED MEDIUM

    FDA 510(k)
    FDA Class 1 ·Hematology

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690122746·Modular Stem 23mm x 125mm

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376676654·Proximity 2-Level ACP, 32 mm

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376656960·Proximity 2-Level X-Lordotic ACP, 32 mm

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376676678·Proximity 2-Level ACP, 32 mm

    Proximity

    FDA UDI
    ALPHATEC SPINE, INC.·00190376676661·Proximity 2-Level X-Lordotic ACP, 32 mm

    RIGIFLEX SINGLE-USE ACHALASIA BALLOON DILATOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Radifocus Optitorque Angiographic Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 5, 2014

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2010

    GOLVO 7007 LOWBASE

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·November 5, 2012

    OPTITORQUE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·Product code DQO·January 20, 2021