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

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    DIGITAL CRADLE

    FDA 510(k)
    FDA Class 1 ·Radiology

    DECT Telephone HAC Communicator

    FDA UDI
    Lifeline Systems Company·00884838081444·DT1000A Refurbished Home Communicator

    INTEGRA EXTERNAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AESKULISA CARDIOLIPIN AGM

    FDA 510(k)
    FDA Class 2 ·Immunology

    ENDOPATH** XCEL* BLADELESS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·May 30, 2014

    MUSTANG¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LIT·November 20, 2012

    SYNCHRON® CX9 ALX CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 21, 2010

    VERSYS FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER, TURPEAUX INDUSTRIAL PARK·Product code JDI·March 31, 2016

    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