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

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    NOOSA Anterior Lumbar Plate System;NAMBUCCA Anterior Lumbar Plate System; CAIRNS Anterior Lumbar Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOMET HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304256316·

    Biomet® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868308901·

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111402074·TC KELLY SCISS STR 6 1/4 INCHES

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·April 20, 2022

    DSS STABILIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OXYLOG 3000 PLUS WORKSTATION, OXYLOG 3000 PLUS BASIC DEVICE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CADD PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·November 30, 2021

    LEGACY PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·March 2, 2022

    CASSETTE MEDI RESERVOIR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·December 10, 2021

    PUMP CADD LEGACY

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·December 14, 2021

    CASSETTE MEDI RESERVOIR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·January 14, 2022

    3012307300-2022-02949

    FDA Adverse Event
    Malfunction ·NULL·Product code FRN·February 8, 2022

    CASSETTE MEDI RESERVOIR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·February 23, 2022

    CADD PUMP AND CASSETTE LEGACY

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·December 9, 2021

    CADD

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·February 7, 2022

    CASSETTE MEDI RESERVOIR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·February 4, 2022

    ENDURANT II

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·June 11, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·September 2, 2008

    US ELITE SYSTEM ELEMENTS

    FDA Adverse Event
    Other ·GYRUS ACMI, INC.·Product code HIH·June 10, 2011