BEUDAMED
    11 results · 37ms · Sources: EU EUDAMED, US FDA

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    MOORE TRACHEOSTOMY TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VERTE-STACK® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074524719·SPACER 2962240 CAPSTONEL PEK VBSEND40X12

    CAREVENT

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

    ProMedTek Model C1400 Shortwave Diathermy Device

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VISTA BRITE TIP GUIDING CATHETERS

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DQY·February 14, 2013

    PROXIMATE** RELOADABLE LINEAR CUTTER WITH SAFETY LOCK-OUT - THICK

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 18, 2011

    CONNEC F/INSERTION HANDLE F/PFNA

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code LXH·July 28, 2014

    UNICEL DXC 800 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JGS·February 21, 2012

    BA102

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·March 31, 2016

    BA105

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·March 28, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·August 29, 2017