BEUDAMED
    8 results · 18ms · 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.

    KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345

    FDA 510(k)
    FDA Class 2 ·Radiology

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B58210512580·HOLDER, NEEDLE, GASTROENTEROLOGIC

    BX TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM

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

    TC-PLUS POROUS FEMORAL COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·April 10, 2013

    HUTIV TABLE ASSY REV W/COLOR

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO·Product code KQS·May 22, 2008

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·April 6, 2011

    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