BEUDAMED
    10 results · 35ms · Sources: EU EUDAMED, US FDA

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    PALL FIELD MEDICAL OXYGEN GENERA. & DISTRI. SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867523456·Spine Compression Screw, 3.5x26mm

    SENTIO MMG Gen 2

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    AMICAS VISION SERIES PACS, MODEL 5.5

    FDA 510(k)
    FDA Class 2 ·Radiology

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·June 14, 2014

    UNKNOWN DEPUY SROM SLEEVE

    FDA Adverse Event
    Injury ·DEPUY (IRELAND)·Product code JDI·December 14, 2012

    EXCEL CONSOLE WITH FOOTSWITCH EACH 1

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES (IRELAND) LTD·Product code LFL·September 22, 2010

    BOLT FOR FEMORAL NECK SYSTEM 85MM LENGTH-STERILE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·April 16, 2020

    BOLT F/FEM NECK SYST F/CONSTRUCT LENGTH

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KTT·October 23, 2019

    SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024