BEUDAMED
    2,940 results · 28ms · Sources: EU EUDAMED, US FDA

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    HY-BOND RESIGLASS

    FDA 510(k)
    FDA Class 2 ·Dental

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741118550·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674111855060·

    Screw for C-Arc

    FDA UDI
    Noras MRI products GmbH·04251269204869·

    Flexitron

    FDA UDI
    Nucletron B.V.·08717213026964·Flexitron Transfer Tube for 4F Flexibles (5)

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587C11185540·11mm H x 18mm W x 55mm L x 4 degree XLIF Corona...

    WAMPOLE HS-CRP ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    PROFAST+ ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    GUARDIAN ROLLING WALKER

    FDA Adverse Event
    Malfunction ·A&E·Product code ITJ·November 4, 2008

    PROMUS ELEMENT¿ PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·May 14, 2013

    CYCLESURE BIOLOGICAL INDICATOR

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code FRC·August 13, 2008

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 27, 2021

    Plum XL3D, list #s 11855-04-01, 11855-04-03, 11855-04-05, 11855-04-07; AC cord manufactured by Electri-Cord, Westfield PA, Infusion pumps manufactured by Hospira, Morgan Hill, CA.

    FDA Recall
    Terminated ·Hospira Inc·Product code FRN·August 11, 2009

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 20, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 14, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 6, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 5, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·September 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 24, 2021