BEUDAMED
    9 results · 19ms · 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 ×

    WITTICH NITINOL STONE BASKET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    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

    DANA REUSABLE TEST PACK FOR STEAM STERILIZATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PRECISA BIOPSY NEEDLE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 30, 2014

    ESSURE

    FDA Adverse Event
    Malfunction ·Product code HHS·November 12, 2010

    TOTALCARE BED

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

    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