BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    STELLAR Knee

    FDA 510(k)
    FDA Class 2 ·Neurology

    STINGRAY LP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·March 26, 2025

    Symetrex LTHD Catheter, Symetrex LTHD Catheter with Sideholes

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RATTAN IMACS BY RATTAN INFORMATION CORPORATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    STINGRAY LP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·February 3, 2025

    STINGRAY? LP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·May 29, 2026

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·November 4, 2008

    ENDOSCOPIC MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 2, 2011

    COROX OTW 75-UP STEROID

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NKE·July 17, 2013

    S-ICD SYSTEM

    FDA Adverse Event
    Malfunction ·CAMERON HEALTH·Product code LWS·June 28, 2017

    ACHIEVE ADVANCE MAPPING CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DRF·August 11, 2023