BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    CURVILINEAR SILICONE CHIN IMPLANT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MINI HARPOON

    FDA UDI
    Biomet Sports Medicine, LLC·00880304464810·

    ACETABULAR PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CINESCOPE III RADIOGRAPHIC GENERATOR

    FDA 510(k)
    FDA Class 1 ·Radiology

    M2A-MAGNUM MOD HD SZ 52MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 30, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC., USA·Product code LFR·October 26, 2007

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·November 29, 2012

    WITTICH NITINOL STONE BASKET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LQR·February 20, 2019

    WITTICH NITINOL STONE BASKET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LQR·February 20, 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