BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    L.A.S.P. LUMBAR AND SACRAL PAD, REPOSITION. SNAP

    FDA 510(k)
    FDA Class 2 ·Neurology

    ALTA HOLLOW TIBIAL RODS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PROXIMATE ILS STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 26, 2014

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 4, 2013

    CYSTOCARE GOLD

    FDA Adverse Event
    Injury ·COLOPLAST MANUFACTURING US, LLC·Product code NNW·November 11, 2010

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021