BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    CLEARPATH UPPER GI

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CapSure® Spine System

    FDA UDI
    Spine Wave, Inc.·10840642104233·Offset Connector Open 40mm

    CLEARCUT S SAFETY KNIFE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    CHEETAH RELIANT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VILEX

    FDA Adverse Event
    Malfunction ·VILEX, INC.·Product code JDW·June 4, 2012

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·March 8, 2018

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·May 9, 2013

    TOTAL ASR FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·May 20, 2011

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code FKX·August 12, 2008

    DEKA SMARTXIDE² TRIO

    FDA Adverse Event
    Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 31, 2023