BEUDAMED
    8 results · 18ms · 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 ×

    AQUA PATCH

    FDA 510(k)
    FDA Unclassified ·Unknown

    Orbitum Bone Staple Implant, X and VI

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COSTORSOL

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

    CODMAN DISPOS PERFORATOR

    FDA Adverse Event
    Injury ·RAYNHAM·Product code HBF·August 8, 2023

    PINN 100 W/GRIPTION 50MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·February 22, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 18, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·August 1, 2014

    Acumatch L-Series BIPOLAR LINER, 22mm (BIPOLAR ENDOPROSTHESIS-Hip), Item Numbers: a) 100-22-19, SZ. L; b) 100-22-20, SZ. M; c) 100-22-21, SZ. N; d) 100-22-22, SZ. P; e) 100-22-23, SZ. R; f) 100-22-24, SZ. S; g) 100-22-25, SZ. T

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·July 10, 2024