BEUDAMED
    13 results · 28ms · Sources: EU EUDAMED, US FDA

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    AMUCHINA

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Barco

    FDA UDI
    Barco NV·05415334029286·Surgical color monitor

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690124245·Modular Offset Stem 13mm x 100mm x 2mm

    Xenco Medical Cervical Interbody System (Argus)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEMASHIELD PLATINUM WOVEN DOUBLE VELOUR TAAA GRAFT CONFIGURATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·May 20, 2015

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·May 22, 2015

    PREMICATH

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·April 20, 2015

    PREMICATH

    FDA Adverse Event
    VYGON GMBH·Product code LJS·April 20, 2015

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·June 3, 2015

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 7, 2011

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.8010379·Product code JDI·July 23, 2014