BEUDAMED
    13 results · 23ms · Sources: EU EUDAMED, US FDA

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    ANA/LITE-RL TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690192138·Apex Revision Knee Reamer – ZIMMER SHORT FLUTES...

    Megasystem C

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575384310·Stem Components,Coupling Component for total fe...

    Ebony PTA .014 RX Pheripheral Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BELLCO SINGLE NEEDLE DOUBLE HEAD PUMP

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    FOLFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 5, 2014

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 4, 2010

    RECEPTAL CANISTER 1000 ML CE

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD, HOSPIRA INC.·Product code GCX·November 12, 2012