BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    Global Modular Replacement System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ImmunoCAP Gliadin IgG Control High

    FDA UDI
    Phadia AB·07333066019925·ImmunoCAP Gliadin IgG Control High

    MEDOS HILITE 7000 & 7000 LT OXYGENATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Reprocessed Inquiry Steerable Diagnostic EP Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CARPENTIER-EDWARDS PERIMOUNT MAGNA AORTIC BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code LWR·November 13, 2008

    VERIFLEX (TM)

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·September 2, 2011

    DEVICE, ELECTROSURGICAL, CUTTING & COAG & ACC.

    FDA Adverse Event
    Malfunction ·Product code GEI·July 18, 2013

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM - DUAL PORT 22 GA 1.00 IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 3, 2020

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·February 24, 2020

    ALIYA

    FDA Adverse Event
    Injury ·NEAUVIA NORTH AMERICA, INC·Product code GEX·May 5, 2026