BEUDAMED
    41 results · 22ms · Sources: EU EUDAMED, US FDA

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    INTERLOCK FIBERED IDC OCCLUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169413696·BLADE 5102912 29MM WIDE VESSELBLADE 12CM

    OTHER EXTERNAL FIXATION

    FDA UDI
    Smith & Nephew, Inc.·03596010031846·8MM SOCKET WRENCH SMALL BONE FIXATOR

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964076978·The ENDO CARRY-ON Procedure Kit contains all of...

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707094548·IMPLANT 2.9 W/CAP D2,9 L12MM

    Verifine

    FDA UDI
    Promisemed Medical Devices Inc.·00850011833582·The proposed device Insulin Syringe, a sterile ...

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707094920·IMPLANT 2.9 W/CAPS D2,9 L12MM

    Mariner MIS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981293505·Bevel Stylet, Shank

    DISPOSABLE NERVE STIMULATING PROBE, BIPOLAR CONCENTRIC, DISPOSABLE NERVE STIMULATOR PROBE, BIPOLAR SIDE BY SIDE

    FDA 510(k)
    FDA Class 2 ·Neurology

    VAGINAL PORT, NON-STERILE / 600065, VAGINAL PORT, STERILE / 600073

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

    Plateau Spacer System

    FDA UDI
    Life Spine, Inc.·00190837026899·PLATEAU Interbody, Curved, Bulleted, 11mm 29mm ...

    HLM TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 1, 2015

    VKMO 70000 #QUADROX-I HMO 70000+VHK71

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 23, 2015

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 30, 2025

    BO-HQV 70600#ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 19, 2015

    BO-HQV #70600ADULT PACK

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DTN·March 4, 2015

    BO-HQV 70600#ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·March 27, 2015

    BO-HQV 70600#ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·April 9, 2015

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·December 4, 2012

    VKMO 11000

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 24, 2015