BEUDAMED
    27 results · 22ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Radiology

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676220408000·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676220408150·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676220408070·

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·34546540355608·Bone Screws, Cross-Pin

    VitaVitro® Fertilization Medium, VitaVitro® Gamete Buffer Medium, VitaVitro® Flushing Buffer Medium

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SYSTEM 2000 CONTROLLER, SYSTEM 5000 CONTROLLER, FOOTSWITCH, POWER CORD, AND VISAGE WANDSFF

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    INRATIO2

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code JPA·October 5, 2009

    INRATIO2

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·December 4, 2009

    INRATIO2

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·December 4, 2009

    INRATIO2

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·December 4, 2009

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·November 4, 2009

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·December 4, 2009

    STARCLOSE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·November 4, 2008

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 23, 2011

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 11, 2013

    EasyPoint Needle, 25G x 5/8", REF: 82091

    FDA Enforcement
    Class II ·Ongoing·Retractable Technologies, Inc.·March 20, 2024

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·January 15, 2010

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code JPA·November 19, 2009

    INRATIO2

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·December 8, 2009