BEUDAMED
    48 results · 25ms · Sources: EU EUDAMED, US FDA

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    SAVINA 300 SAVINA 300, COUNTRY VARIANTS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DSC/ALF SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OLYMPUS ULTRASONIC GASTROVIDEOSCOPE GF TYPE UC140P-DO5 & OLYMPUS ULTRASONIC GASTROFIBERSCOPE GF TYPE UC30P

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

    TARGETING ARM PROX. LAT. TIBIA LEFT

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·February 2, 2012

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NDN·March 28, 2013

    ON-Q EXPANSION KIT: SILVERSOAKER 10 IN

    FDA Adverse Event
    Injury ·I-FLOW, LLC·Product code BSO·May 15, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 9, 2011

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·August 13, 2008

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NDN·February 27, 2013

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NDN·March 1, 2013

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NDN·February 27, 2013

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code OKS·August 19, 2014

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 13, 2017

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 5, 2017

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016