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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    SURGICAL DRAPES AND ACCESSORIES USING PEBAX FILM

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

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556700676·GC Initial™ MC Cervical Transluc. CT-24, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228701241·GC Initial™ MC Cervical Transluc. CT-24, 20g

    Level One Hand Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GASTROSTOMY REPLACEMENT TUBE, MODEL 253

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

    WALKMED® 150 ML RESERVOIR BAG

    FDA Adverse Event
    Malfunction ·WALKMED TECHNOLOGIES, LLC·Product code FRN·September 5, 2025

    LUXSTAR CEILING MOUNT LIGHT

    FDA Adverse Event
    Malfunction ·MARUS·Product code EAZ·April 29, 2014

    PUMP MMT-712NAB PRDGM INSULIN BL EN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·October 11, 2010

    EEA 31MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC PUERTO R·Product code GDW·December 4, 2012