BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    ACUSON NX2 Diagnostic Ultrasound Systems

    FDA 510(k)
    FDA Class 2 ·Radiology

    DUOLINK II

    FDA 510(k)
    FDA Class 2 ·Dental

    MAXFORCE TTS SINGLE-USE BALLOON DILATOR

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

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 19, 2013

    LOGIC TIBIA PS MOD INSRT SZ 1 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·March 1, 2023

    REVEAL LINQ

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code DSI·October 10, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·July 8, 2011

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE GO GEAR BELT

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·June 6, 2013

    BD¿ NEXIVA SINGLE PORT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 21, 2019