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

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    EL-ACL SCREEN; EL-ACL IGM, IGG, IGA

    FDA 510(k)
    FDA Class 2 ·Immunology

    CALEX CONDITIONER

    FDA 510(k)
    FDA Class 2 ·Dental

    HDR MIAMI APPLICATOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    LUMOS DR-T

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO,·Product code LWS·August 30, 2006

    KENTROX SL 65/16

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code LWS·August 30, 2006

    UNKNOWN NOTTINGHAM SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code MBF·May 17, 2017

    COMPREHENSIVE SHOULDER SYSTEM MODULAR HEAD - VARIABLE OFFSET 42MM X 18MM X 46MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HSD·October 19, 2016

    SYNERGY

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 16, 2013

    DELTAPLUSH - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR, LLC·Product code HCG·September 4, 2014

    M2A RINGLOC ACETABULAR LINER 28MM SIZE 25 STANDARD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·April 15, 2011

    KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE

    FDA 510(k)
    FDA Class 2 ·Neurology