BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    LEGIONELLA PNEUMOPHILA SER. 1 ANTIGEN LATEX TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    P.F.C.

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295216322·P.F.C. NON-POROUS KEEL TIBIAL TRAY SZ 1 58mm M/...

    BRUCELLA MEDIA

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PLASTELAST AND/OR ELASTOPLASTE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    COBAS 8000 C702 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·June 10, 2014

    VITROS CHEMISTRY PRODUCTS IMMUNO-WASH FLUID

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·December 10, 2012

    PINN CAN BONE SCREW 6.5MMX25MM

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code LPH·June 23, 2015

    Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026