BEUDAMED
    8 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 ×

    OSTEOGUIDE ANORGANIC BONE MINERAL PRODUCTS

    FDA 510(k)
    FDA Class 2 ·Dental

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496043034·RELAX UNISEX 140, SIZE XXL, CORDA, GRADUATED CO...

    MODIFICATION TO: THERMACOOL IIA

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

    COLTENE AURA COMPOMER RESTORATIVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    AUGOLUBE - III W/FOOT CONTROL

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code GEY·March 7, 2013

    THERMOPHORE ARTHRITIS PAD

    FDA Adverse Event
    Malfunction ·BATTLE CREEK EQUIPMENT COMPANY·Product code IRT·March 15, 2011

    VENTAK PRIZM HE DR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 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