BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    MASS SPECTROMETRY MONITORING LINE CONONECTORS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL

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

    GESCO PER-Q-CATH CATHETER INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WORKHORSE II BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS, INC.·Product code LIT·June 25, 2007

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 29, 2019

    UNKNOWN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·January 22, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·July 10, 2014