BEUDAMED
    46 results · 24ms · Sources: EU EUDAMED, US FDA

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    AUTOMATIC BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    A.S.A.P.® Bulk Pack Small Final High Shine Polisher

    FDA UDI
    DEN-MAT HOLDINGS, LLC·00359883003531·Dental abrasive disk

    A.S.A.P. Bulk Pack Small Final High Shine Polisher

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172019309·Dental abrasive disk

    ZEUS-O

    FDA UDI
    SPINAL ELEMENTS·00840916122348·Zeus-O Implant, 13 x 9 x 25mm

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311309250·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16710031309250·

    ASCENSION ANKLE FUSION NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROXIMATE HCS HEMORRHOIDAL CIRCULAR STAPLER AND ACCESSORIES, MODEL PPH01

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    3.5FR URETHANE UMB CATH

    FDA Adverse Event
    Malfunction ·COVIDIEN MANUFACTURING SOLUTIONS SA·Product code FOS·September 9, 2014

    1.9F ARGYLE SINGLE LUMEN PICC

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code LJS·September 18, 2014

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 24, 2023

    3.5FR P.U.R. UMBIL CATH X10

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FOS·June 3, 2014

    2.5FR URETHANE UMB CATH

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FOS·May 29, 2014

    3.5FR URETHANE UMBCATH

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FOS·June 17, 2014

    2.5FR URETHANE UMB CATH

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FOS·May 29, 2014

    3.5FR P.U.R. UMBIL CATH X10

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FOS·November 7, 2014

    3.5FR P.U.R. UMBIL CATH X10

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FOS·October 3, 2014

    3.5 FR URETHANE UMB CATH

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FOS·July 28, 2014

    DUAL LUMEN INSERTION TRAY

    FDA Adverse Event
    Malfunction ·COVIDIEN, COVIDIEN MANUFACTURING·Product code LJS·September 18, 2014

    DUAL LUMEN INSERTION TRAY

    FDA Adverse Event
    Malfunction ·COVIDIEN, COVIDIEN MANUFACTURING·Product code LJS·September 18, 2014