BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    MODEL 7320 VISUAL STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    Rapid-i™ Kit

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ANALYZER-SUPPLEMENT, KINETIC, LKB 2086

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·April 30, 2014

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 10, 2012

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 3, 2010

    Tobii C-Series Lithium batteries Type TB8A, TB8B, TB12A used with the Tobii C8 and Tobii C12 Speech Generating Communication Devices. Communication device for the impaired and functions as a speech generating device; text or symbols can be used to generate synthesized or digitized speech. Perfect for asking or answering questions, having a conversation.

    FDA Recall
    Terminated ·Tobii Assistive Technology, Inc.·Product code ILQ·May 31, 2011