BEUDAMED
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    'CATCH-IT' OR FECAL CONTAINMENT DEVICE

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    MULTIANALYTE CONTROLS-ALL KINDS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CipherOx CRI M1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYMBIQ SCHANNEL 3.01

    FDA Adverse Event
    HOSPIRA COSTA RICA LTD.·Product code FRN·May 29, 2014

    LINEAGE® TRANSCEND® CERAMIC ACETABULAR LINER

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MRA·December 14, 2012

    MA204

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL QUEBEC LP·Product code FNL·September 29, 2010

    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