BEUDAMED
    11 results · 20ms · 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.
    Filters Regulation: Us FDA ×

    BIFURCATED GORE TEX STRETCH VASCULAR GRAFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TO GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    NEEDLE-SHIELD

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRA.SPEC NON-STERILE LATEX EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GMK-PRIMARY FEMUR STD CEMENTED SIZE 4 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 3, 2021

    LIFTLOC SAFETY INFUSION SET

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code FMI·June 23, 2014

    ULTRAFLEX¿ TRACHEOBRONCHIAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code JCT·January 9, 2013

    SINGLE 8 EXTENSION

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·October 28, 2010

    STEALTHSTATION¿ S8 SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·September 19, 2025