BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    SPINAL POSITIONING FRAME

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MICRO WORKTABLE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    HAELAN 340 MUSCLE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    WRIGHT MEDICAL TECHNOLOGIES SIZE 52MM LINEAGE SOLID ACETABULAR COMPONENT

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL·Product code KWA·January 14, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010

    PRISMAFLEX M100 SET

    FDA Adverse Event
    Injury ·GAMBRO INDUSTRIES·Product code KDI·July 9, 2014

    Zeiss brand IOLMaster, Version 1-5, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufactured by Carl Zeiss Meditec AG (Jena), Carl Zeiss Promenade 10, Jena, Germany 07745; and distributed by Carl Zeiss Meditec, Inc., Dublin, CA This device is intended for use primarily by physicians and health care workers and may be only used under the supervision of a physician. This device will not be sold to the general public. The IOLMaster is intended for the biometric determination of ocular measurements of axial length, anterior chamber depth, corneal radius, white-to white (WTW), and for the measurement of pupil size and deviation of the visual axis from the center of the pupil. For patients who are candidates for intraocular lens (IOL) implantation, the device also performs calculations to assist physicians in determining the appropriate IOL power and type for implantation

    FDA Enforcement
    Class II ·Terminated·Carl Zeiss Meditec, Inc.·November 27, 2013