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

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    RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DISPOSABLE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Neurology

    LOSS OF RESISTANCE SYRINGE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SINGLE EXTENSION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 5, 2013

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MEDTRONIC SINGAPORE OPERATIONS·Product code DTB·October 10, 2014

    PIN COLLET

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code GET·May 19, 2011

    BD¿ NEXIVA SINGLE PORT

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

    OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial Components (Product Line: 02-012-38-XXXX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021