BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS

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

    BODIHEALTH SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    SMITH & NEPHEW DYONICS ELECTROBLADE RESECTOR

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

    MIS QUAD-SPARING INSERTER/EXTRACTOR PAD

    FDA Adverse Event
    Malfunction ·ZIMMER INC.·Product code LXH·November 22, 2010

    ASR UNI FEMORAL IMPL SIZE 55

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 28, 2013

    ITREL 3

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·July 14, 2014

    RATCHETING SCREWDRIVER HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·December 12, 2022