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

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    Ki Power Tilt System

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704002543·CODMAN Slimline Temporary Aneurysm Clip No 7 Bl...

    Puget Sound Energy - 18 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588014692·Puget Sound Energy - 18 Metal

    DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    OWL RADIOFREQUENCY SYSTEM, MODEL URF-2AP

    FDA 510(k)
    FDA Class 2 ·Neurology

    Widex

    FDA UDI
    Widex A/S·05706069728354·Widex EVOKE E-FS (Autumn Beige S-440 ) Telecoil...

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·October 27, 2014

    MAXIMO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2011

    MAQUET SAS

    FDA Adverse Event
    Malfunction ·MAQUET SAS- ORLEANS- FRANCE·Product code FSY·June 26, 2013

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·March 16, 2018

    EMBLEM MRI S-ICD pulse generators, as part of Boston Scientific S-ICD System; Model A219

    FDA Enforcement
    Class II ·Ongoing·Boston Scientific Corporation·February 3, 2021