BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    SKINSENSE POLYISOPRENE UNDERGLOVE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    TEMPORARY PACEMAKER EXTENSION CABLE, MODELS 5235, 5235A, 5235V, TEMPORARY PACEMAKER SURGICAL EXTENSION CABLE, MODELS 528

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CT/MASTER, VERSION 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·December 30, 2024

    CORAIL2 NON COL HO SIZE 10

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS-3003895575·Product code MEH·April 26, 2013

    STEALTHSTATION TREON TREATMENT GUIDANCE SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·April 21, 2011

    SHILEY DISPOSABLE LOW PRESSURE CUFFED

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TYCO HEALHCARE·Product code BTO·July 23, 2008

    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