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

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    BIOSIGN(TM_ RUBELLA - RUBELLA ANTIBODY TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111116·KATENA INSTRUMENT RACK

    ADS-GEL AND INSULATING-GEL

    FDA 510(k)
    FDA Class 2 ·Dental

    BROAD SELF-COMPRESSING PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·January 17, 2013

    REDUCTION FORCEPS WITH SERRATED JAW-RATCHET 144MM

    FDA Adverse Event
    Malfunction ·SYNTHES TUTTLINGEN·Product code HTD·July 10, 2014