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    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC01001·ROD, CURVED BULLETED, 5.5 X 100MM

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC00351·ROD, CURVED BULLETED, 5.5 X 35MM

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC01301·ROD, CURVED BULLETED, 5.5 X 130MM

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC00901·ROD, CURVED BULLETED, 5.5 X 90MM

    ARC Handpiece Small Threaded Cannula

    FDA UDI
    MENTOR TEXAS L.P.·00081317020455·ARC Handpiece Small Threaded Cannula

    ARC Handpiece Large Threaded Cannula

    FDA UDI
    MENTOR TEXAS L.P.·00081317020448·ARC Handpiece Large Threaded Cannula

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC00751·ROD, CURVED BULLETED, 5.5 X 75MM

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC00651·ROD, CURVED BULLETED, 5.5 X 65MM

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·14026704661982·14FR Red Rubber Coude

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC00701·ROD, CURVED BULLETED, 5.5 X 70MM

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC00451·ROD, CURVED BULLETED, 5.5 X 45MM

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC01201·ROD, CURVED BULLETED, 5.5 X 120MM

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC01101·ROD, CURVED BULLETED, 5.5 X 110MM

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·04026704552245·14FR Red Rubber Coude

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC01401·ROD, CURVED BULLETED, 5.5 X 140MM

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC00401·ROD, CURVED BULLETED, 5.5 X 40MM

    Cosmolock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310BRC00801·ROD, CURVED BULLETED, 5.5 X 80MM

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·FACT(TM)AND ARC BALLOON CORNARY DILATATION CATHETERS

    BRC SOFTWARE PRODUCT

    FDA 510(k)
    FDA Class 2 ·Neurology

    VERIFY

    FDA UDI
    STERIS CORPORATION·00724995023904·The VERIFY Vial Activator Set is used with the ...