BEUDAMED
    9 results · 38ms · Sources: EU EUDAMED, US FDA

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    MULTIPLE NAME MODEL MULTIPLE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    AESCULAP SPIEGELBERG BRAIN PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    MSS-28CS-301/701 NEEDLESCOPE

    FDA 510(k)
    FDA Class 2 ·Neurology

    NV MICROCATHETER

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·July 9, 2020

    MALLINCKRODT

    FDA Adverse Event
    Injury ·COVIDIEN·Product code BTR·April 30, 2013

    FLEXIVA (TM) HIGH POWER SINGLE-USE LASER FIBER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEX·September 16, 2014

    ARCHITECT HAVAB IGM REAGENT

    FDA Adverse Event
    Malfunction ·ABBOTT·Product code LOL·May 18, 2011

    BD CONNECTA¿ STOPCOCK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·February 14, 2019

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012