BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    PORGES STEPPED NEOPLEX DILATOR

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

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867047341·LO-PRO SCRW TM,SS 3.5X 26MMCORT

    K083526

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·May 7, 2018

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 20, 2021

    TRILOGY 100 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Codman Electrosurgical Generator, Foot Pedal

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ANTEROLAT DIST TIB PLT, SS, RIGHT, 16H

    FDA Adverse Event
    Injury ·ARTHREX INC.·Product code HRS·June 14, 2018

    ACCU-CHEK ® AVIVA COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·June 19, 2014

    PURELIGHT

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC·Product code DQA·October 19, 2010

    SWAN-GANZ BIPOLAR PACING CATHETER FOR FEMORAL INSERTION

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code LDF·December 21, 2012