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

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    PEDIATRIC QUIK-COMBO

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    INTELLIVUE GAS MODULES, MODELS G5 M1019A AND G1 M1013A

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    In2Bones Kirschner wire

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·January 7, 2011

    UNIFY ASSURA CRT-D

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·July 23, 2014

    3.5MM LCP PERIARTICULAR PROX HUMERUS PL 4 HOLE/127MM/RT

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·October 25, 2018

    STEALTH 32 LHOOK LAP ELEC PKG

    FDA Adverse Event
    Malfunction ·CONMED UTICA·Product code GEI·November 12, 2021

    STEALTH 32 LHOOK LAP ELEC PKG

    FDA Adverse Event
    Malfunction ·CONMED UTICA·Product code GEI·November 12, 2021

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026