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

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    VARIANT BETA-THALASSEMIA SHORT PROGRAM

    FDA 510(k)
    FDA Class 2 ·Hematology

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981240318·Trial, 9mm x 24mm x 12mm, 22 Deg

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981239909·Interbody, 9mm x 24mm x 12mm, 22 Deg

    ORTHO ARCH

    FDA UDI
    Ortho Arch Company Inc·D90992412217·.022 L6L SINGLE CONVERTIBLE -25T DIRECT BOND (5)

    INSYTE-A ARTERIAL CATHETERIZATION UNIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NAUTICA MICRO CATHETER, MODEL 105-5094-153

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    UNKNOWN DEPUY METAL LINER

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ? REG. # 8010379·Product code KWY·January 22, 2013

    ATTAIN OTW

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

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010