BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    APR II HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INJEKT CYSTO FLEXIBLE INJECTION NEEDLE

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

    BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK

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

    DRILL F.RADIOLUCENT TARGETING DEVICE SIDEWINDER Ø3,2 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·September 16, 2013

    MULTI SPECT 2 [510(K) K913630]

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS·Product code IYX·April 13, 2001

    VASCUCLEAR PRECISION BIPOLAR

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code GEI·January 7, 2013

    RECONSTITUTION DEVICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code FPA·December 3, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·July 3, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 24, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 26, 2015

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 5, 2015