BEUDAMED
    228 results · 29ms · Sources: EU EUDAMED, US FDA

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    Lucent Intervertebral Body Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707013914·CALIBRA 1ST MOL BANDS W/G8325-02 n.UR 11

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528128930·2.0mm x 11mm Cannulated Headless Screw

    LACTOSORB* 2.0MM SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036053949·

    ECLIPSE TREATMENT PLANNING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    PILONPLATE WITH ANGULAR STABILITY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DERMABOND UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code MPN·October 17, 2018

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·October 17, 2018

    IMPLANTMED SI-915, 2011

    FDA Adverse Event
    Injury ·W&H DENTALWERK BUERMOOS GMBH·Product code EBW·September 5, 2018

    IMPLANTMED SI-915, 2011

    FDA Adverse Event
    Malfunction ·W&H DENTALWERK BUERMOOS GMBH·Product code EBW·August 14, 2018

    CARELINK

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·June 7, 2013

    CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·July 7, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 8, 2014

    SPARE MOTOR COMPLETE, IMPLANTMED SI-915, 2011, 1.8 M

    FDA Adverse Event
    Injury ·W&H IMPEX INC.·Product code EBW·July 31, 2018

    BD POSIFLUSH¿ IV FLUSH SOLUTION SODIUM CHLORIDE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·December 30, 2021

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 24, 2012

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 24, 2012

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 24, 2012

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 24, 2012

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 24, 2012