BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    myosmart. (13E522); myosmart.cuff (757M20-2); connectgrip. (560X27-1); myosmart trial kit (642V64=T)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Imbio RV/LV Software

    FDA 510(k)
    FDA Class 2 ·Radiology

    3M TEGADERM SILVER (AG) MESH

    FDA 510(k)
    FDA Unclassified ·Unknown

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Other ·MEDTRONIC NEUROMODULATION·Product code MHY·June 6, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 6, 2008

    PISCES QUAD PLUS

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code GZB·June 4, 2008

    PISCES QUAD PLUS

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code GZB·June 4, 2008

    ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 30, 2019

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·November 13, 2014

    UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 9, 2011

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2013

    ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 17, 2019

    OXFORD ANAT BRG LT MD SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·April 17, 2024

    ALINITY I B12 REAGENT KIT

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code CDD·May 14, 2021

    TORQUE LIMITING HANDLE WITH 4.5MM QUICK COUPLING

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·January 27, 2020