BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    PARAMAX SALICYLATE REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    LATEX TUBING-AMBER-5/16 x 1/8"

    FDA UDI
    W.H. Holden, Inc.·D9288330030·

    SUCTION COAGULATOR

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

    RIGHTEST CONTROL SOLUTION

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 25, 2014

    UNKNOWN LEFT HIP

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

    ENVOY 6F GUIDING CATHETERS

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DQY·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