BEUDAMED
    9 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 ×

    HRW-63-INT WRIST ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    Cook

    FDA UDI
    COOK INCORPORATED·00827002269859·Multipurpose Procedure Tray

    OXOID PYLORI TEST KIT, MODEL DR0130M

    FDA 510(k)
    FDA Class 1 ·Microbiology

    X-IMAGE DIGITAL X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    2022588-1998-00001

    FDA Adverse Event
    Injury ·Product code DSI·August 18, 1998

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 27, 2013

    MEDISENSE OPTIUM

    FDA Adverse Event
    Malfunction ·Product code NBW·March 17, 2011

    N'VISION

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·April 1, 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