BEUDAMED
    337 results · 31ms · Sources: EU EUDAMED, US FDA

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    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00812277036336·Airway Kit, Supraglottic W/Et Holder, size 4

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00810071631412·Capnoline Multi Pack Kit (includes 10 #177268) ...

    Thermoflect

    FDA UDI
    Encompass Group, L.L.C.·00612899004375·THERMOFLECT BLANKET, L, 25EA ...

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00810071631375·Kit, Sam Junctional Tourniquet Deployment Modul...

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00812277036404·Assure Prism Orange Kit ADVANCED

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00812277037142·Curaplex Basic Blood Transfusion Kit (Fed Gov)

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00810071631429·Curaplex Single-Dose Opioid Overdose Kit, Bagge...

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00810071631405·GO-PAP with Neb-Connect Capno Kit: Adult Med Ma...

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00810071631382·Nio Kit, Adult (Fed Gov)

    CONMED

    FDA UDI
    Conmed Corporation·10845854045749·Electrosurgical Apparatus, System 5000 Army Kit...

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00812277036398·Curaplex Opioid Overdose Kit, Single Dose

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00810071631399·Nio Kit, Pediatric (Fed Gov)

    OPTIFLUX 180NRE DIALYZER FINISHED ASSY.

    FDA Adverse Event
    Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·March 19, 2021

    Curaplex

    FDA UDI
    BOUND TREE MEDICAL, LLC·00812277036558·Curaplex DOD Officer Down Basic IFAK

    THIRD DEVICE: REVERE LOCKING CAP

    FDA Adverse Event
    Injury ·GLOBUS MEDICAL, INC.·Product code NKB·May 20, 2010

    SECOND DEVICE: 7.0MM REVERE DUAL OUTER DIAME

    FDA Adverse Event
    Injury ·GLOBUS MEDICAL, INC.·Product code NKB·May 20, 2010

    FIRST DEVICE: 7.0MM REVERE DUAL OUTER DIAMETER

    FDA Adverse Event
    Injury ·GLOBUS MEDICAL, INC.·Product code NKB·May 20, 2010

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code NVZ·January 8, 2019

    MEDTRONIC LEAD

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·January 8, 2019

    CEPHEID XPERT XPRESS SARS-COV-2 DOD

    FDA Adverse Event
    Malfunction ·CEPHEID·Product code QJR·February 17, 2022