BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

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    PARAMAX BILIRUBIN CALIBRATORS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AUTOCLAVABLE, LATEX SILICONE TUBING GREY, 1/4" I.D. x 3/32" WALL

    FDA UDI
    W.H. Holden, Inc.·D9288330050·

    LM-Dental 833005

    Device
    EU MDR · Eu Md Class 1 ·LM-Instruments Oy·Not intended for eu market

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0330050·Vise Grip, Large, 5.5mm

    MFGD 1318 18 INCH 1 MEGAPIXEL GREYSCALE LCD DISPLAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    HEMOSIL VON WILLEBRAND ACTIVITY ASSAY

    FDA 510(k)
    FDA Class 2 ·Hematology

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·May 27, 2014

    UNKNOWN ACCOLADE STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·October 30, 2012

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·September 14, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018