BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    INFANT CANNULA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    O.I.C. TITANIUM

    FDA UDI
    Stryker Corporation·07613327261875·ROOT RETRACTOR

    UCSS® Screw Set

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978067759·CASE 873-012 UCSS INSTRUMENT MODULE

    Legacy™4 Healing Collar-Concave Profile

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307112211·

    SHUR-PATCH TAPE PATCH

    FDA 510(k)
    FDA Class 2 ·Neurology

    ANGIO-PRESS LITE DVT Compression Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 13, 2014

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 18, 2010

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 13, 2012

    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