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

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    Filters Regulation: Us FDA ×

    WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    All’InCath 035M PTA Balloon Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 6, 2013

    SENSIA DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014