BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    MMH PTH RIA KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NBX

    FDA UDI
    NUTEK ORTHOPAEDICS INC·B488830700000·NON-BRIDGING EXTERNAL FIXATOR HAND SHORT

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971666·

    RIWOtrack Navigation System

    FDA 510(k)
    FDA Class 2 ·Neurology

    CERALAS D 10-60 810NM LASER SYSTEM WITH ENDO LASER VEIN SYSTEM KIT

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

    ARGYLE SALEM SUMP TUBE WITH ANTI-REFLUX VALVE

    FDA Adverse Event
    Malfunction ·SHERWOOD DAVIS AND GECK·Product code KNT·August 29, 1996

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 23, 2014

    REPLACEMENT TUBE

    FDA Adverse Event
    Malfunction ·ABBOTT NUTRITION·Product code KNT·November 13, 2012

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015