BEUDAMED
    14 results · 29ms · Sources: EU EUDAMED, US FDA

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    DORNIER MEDILAS H30 SOLVO

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

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970423·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970393·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970492·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172974032·UniTip High Resolution Catheter 12F

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970485·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970416·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970409·

    POWERPICC SV CATHETERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PISTON SYRINGE & HYPODERMIC NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    USA ELITE SYSTEM CONTINUOUS FLOW INNER SHEATH

    FDA Adverse Event
    Injury ·GYRUS ACMI, INC.·Product code HIH·May 17, 2013

    WALLFLEX¿ BILIARY RX STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·September 26, 2014

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 3, 2011

    Maquet PowerLED 700. Product Usage; To provide illumination to the surgical area or the patient.

    FDA Enforcement
    Class II ·Terminated·Maquet Medical Systems USA·June 18, 2014