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

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    SAFETY VEST

    FDA 510(k)
    FDA Class 1 ·General Hospital

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471149892·K-WIRE - DOUBLE TROCAR FULLY THREADED 2.4mm DIA...

    MODIFICATION TO EMBOL-X INTRA-AORTIC FILTER: X-SMALL, SMALL, MEDIUM, LARGE, X-LARGE WITH HEPARIN COATED MESH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZipE Knotless Tissue Repair and Attachment Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OASYS MIDLINE OCCIPUT PLATE- SMALL

    FDA Adverse Event
    Injury ·STRYKER SPINE-FRANCE·Product code KWP·February 14, 2013

    CROSSLINK ANCHOR PG GLENOID 52

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWS·January 7, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014