BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    HELENA FACTOR II DEFICIENT SUB. PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    NEOCIF INSERTION INSTRUMENT

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code MQP·November 6, 2018

    Navigated Anterolateral Disc Prep Instruments

    FDA 510(k)
    FDA Class 2 ·Neurology

    C-THRU SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NEOCIF INSERTION INSTRUMENT

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code MQP·July 20, 2017

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·March 24, 2017

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·May 6, 2014

    NEXGEN LPS FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code NJL·October 12, 2012

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·August 11, 2010

    EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code ODG·December 15, 2021