BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    SYNERGY SCREEN TEST, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Bosworth New Truliner

    FDA UDI
    Harry J Bosworth Company·H66809219771·New Truliner 1 lb bulk PEMA P&L Kit Pink

    PLASMAJET NEUTRAL PLASMA SURGERY SYSTEM

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

    HYBRID FS & HYBRID FS TORIC (HYCOFOCON A) RGP CONTACT LENS FOR DAILY WEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    TARGETING ARM T2 PROX. HUM.

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 27, 2012

    MTS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 4, 2013

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·December 7, 2010

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 9, 2014