BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    Narval Brux

    FDA 510(k)
    FDA Unclassified ·Unknown

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814268·GENUMEDI PT SILVER R III

    NEWDEAL INTERPHALANGEAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    2520274-2013-02954

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·June 3, 2013

    L9000 LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·June 3, 2011

    PINN MAR NEUT 28IDX48OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·August 28, 2008

    GMK PS TIBIAL INSERT SIZE 3 / 17 MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·June 11, 2015