BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    MYOSURE LITE TISSUE REMOVAL DEVICE (1 PACK), MYOSURE LITE TISSUE REMOVAL DEVICE (3 PACK)

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SET, ADMINISTRATION, INTRAVASCULAR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2016

    INFINIX-I INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V

    FDA 510(k)
    FDA Class 2 ·Radiology

    STERILE POLYISOPRENE POWDER-FREE BLUE SURGICAL GLOVES WITH NEU-THERA EMOLLIENT COATING

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    LAP-BAND SYSTEM ACCESS PORT I KIT

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·May 15, 2013

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FSA·September 26, 2014

    UNKNOWN DEPUY 28X50 N LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·June 9, 2011

    MEGA 7.5FR. 40CC

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·February 10, 2020