BEUDAMED
    31 results · 28ms · Sources: EU EUDAMED, US FDA

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    FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMEN

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772003051·HUMERAL FRACTURE BRACE, LEFT, MD

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198970·AK3 Congruent Insert Trial Size 2, 13mm

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482053133·Symmetry® Probe, w/Eye, Stainless Steel, 5 1/8 in

    NA

    FDA UDI
    STERILMED, INC.·10888551018029·BUR CARBIDE MICRO SIDE-CUTTING CROSS-CUT FISSUR...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450437230·

    CONMED

    FDA UDI
    Conmed Corporation·10845854002902·MICRO TAPERED FISSURE BUR, MEDIUM, 2.1 X 4.9 MM...

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962108840·PROBE W/EYE, 5 1/8", SLIVER

    MODIFICATION TO SYNCHRON LX 20 CLINICAL CHEMISTRY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CONCHATHERM 2000 HUMIDIFICATION SYSTEM, MODELS 500-00, -10, -20, -30, -40, -50, & -60

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·December 23, 2014

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·November 22, 2014

    SYNCHRON LX 20 PRO CLINICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·June 8, 2011

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code OVD·April 21, 2018

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·May 10, 2013

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SWINNEA DC·Product code MAX·February 18, 2011

    SOVEREIGN SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code OVD·August 9, 2017

    CLINITEK STATUS+

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code JHI·December 2, 2019

    ACCUTORR V MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 16, 2014