BEUDAMED
    13 results · 33ms · Sources: EU EUDAMED, US FDA

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    VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    Ortho Development Corporation·00822409129713·Uni Knee Keeled Tibial Tray Trial Size 2 Right

    OLYMPUS EMPOWER H65

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM S.P.A.·Product code GEX·May 19, 2022

    XPERT MRSA/SA NASAL ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VU APOD INTERVERTABRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    E-Z CLN L-WR LAP SPLIT STEM 33CM

    FDA Adverse Event
    Malfunction ·MEGADYNE MEDICAL PRODUCTS, INC.·Product code GEI·September 7, 2018

    E-Z CLN L-WR LAP SPLIT STEM 33CM

    FDA Adverse Event
    Malfunction ·MEGADYNE MEDICAL PRODUCTS, INC.·Product code GEI·June 21, 2018

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·January 28, 2026

    CELSIUS¿ THERMO-COOL¿ ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·June 20, 2013

    TURON SHOULDER INSTRUMENT

    FDA Adverse Event
    Malfunction ·ENCORE MEDICAL, L.P.·Product code KWS·April 28, 2011

    CODMAN DISPOSABLE PERFORATOR

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code HBF·September 23, 2008