BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    CLX ACETABULAR CUP (WAGNER) FOR CEMENTLESS FIXAT.

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    AirFit F20

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FLEXGUARD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    WALKMED® 150 ML RESERVOIR BAG

    FDA Adverse Event
    Malfunction ·WALKMED TECHNOLOGIES, LLC·Product code FRN·September 5, 2025

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·June 12, 2014

    HEARTMATE XVE LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·October 7, 2010

    ACCESS

    FDA Adverse Event
    Malfunction ·BIEFFE MEDITAL MANUFACTURING S.A.R.L. TUNIS·Product code FPA·December 12, 2012

    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