BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    FLUSH SOLUTION CONCENTRATE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613252599661·CUSTOMIZED MAND. RECON PLATE20, FULL

    Curette

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102053·MEYERHOEFER CURETTE #2

    Continuum® Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024153462·

    Continuum® Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024153455·

    TEMPERATURE SENSOR CATHETER

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

    FLEXISKIN LATEX EXAMINATION GLOVES, POWDERED, NON STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 23, 2014

    MESH - COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·November 1, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 7, 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