BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    EVACUATION KIT #7-510-14

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

    PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FLU ADMIN/WASTE DISP SYS/PROTEC STA/ADMIN/FLUSH-N-

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NEXGEN LPS-FLEX PROLONG ARTICULAR SURFACE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·July 13, 2015

    CL CONTINU-FLO SOLN SET, 2 LAVS, L/L

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FPA·December 4, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 5, 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