BEUDAMED
    25 results · 25ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Dental

    NITREX™

    FDA UDI
    EV3, INC·00763000185404·GW N180802 NITREX V04

    NITREX

    FDA UDI
    Covidien LP·10821684009069·Guidewire

    NITREX

    FDA UDI
    Covidien LP·00821684058169·Guidewire

    Paxeon Origin

    FDA UDI
    PAXEON RECONSTRUCTION LLC·08177570200337·Origin Stem, Standard Offset Size 8 Collared

    Origin

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215001551·

    n/a

    FDA UDI
    Ortho Development Corporation·00822409067602·Slotted Stem Trial 18x80mm

    Origin Hip Stem

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215051631·

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161111808020·Standard Offset, Collared Stem, Size 8

    NITREX¿

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DQX·July 3, 2018

    NITREX GUIDEWIRE

    FDA Adverse Event
    Injury ·EV3 INC.·Product code DQX·June 30, 2004

    EMAX 2 PLUS SYSTEM, MODEL EMAX 2 PLUS MOTOR, EMAX 2 CONSOLE>FIRMWARE UPGRADE, EMAX 2 FP FOOT PEDAL

    FDA 510(k)
    FDA Class 2 ·Neurology

    AESCULAP IMPLANT SYSTEMS SIBD SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STRATUS Stem

    FDA UDI
    AMPLITUDE SAS·03701089521239·

    EMAX2PLUS

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 1, 2015

    EMAX 2 MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 6, 2015

    LYNX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 20, 2013

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·July 1, 2011

    SILICONE ADVANCED OPTIC-VIOLET SHIELD

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·September 23, 2008

    HS SYNERGY CURVED BLADE

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·April 14, 2021