BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    GESCO PER-Q-CATH CATHETER INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MICROTEK-HERITAGES SILICONE BULB EVACUATION SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ACS THERAPEUTIC DRUG MONIT CONTR, SET I, LEVEL II

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    LEGEND FOOTED ATTACHMENT

    FDA Adverse Event
    Malfunction ·MDT POWERED SURGICAL SOLUTIONS·Product code HBB·December 6, 2010

    DEPUY ASR XL FEM IMP SIZE 57

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 15, 2013

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·July 7, 2014