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

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    LOGIQ E10s, LOGIQ Fortis

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526189737·LEVAMED ACTIVE ANKLE SUP BLACK L IV

    Novo Surgical Inc.

    FDA UDI
    NOVO SURGICAL, INC.·00842331182921·collier needle holder, fenestrated jaws, 5 1/8"...

    IMMEDIATE STABILIZING DEVICE (ISD)

    FDA 510(k)
    FDA Class 2 ·Dental

    MP 719

    FDA 510(k)
    FDA Unclassified ·Unknown

    REVOLUTION CATHETER

    FDA Adverse Event
    Other ·VOLCANO CORPORATION·Product code DQO·October 8, 2008

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·August 5, 2011

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 8, 2013

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code KMW·April 25, 2022

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code KMW·July 7, 2022

    PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL MRI (Model Number L211), EL (Model Number L221), and EL MRI (Model Number L231).

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·January 22, 2025