BEUDAMED
    12 results · 22ms · 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.

    Emily's Care Nourish Test System (Model 1)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    M.U.S.T. PEDICLE SCREWS SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025

    Disposable Surgical Gown

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

    Ankle Truss System (ATS)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·January 13, 2026

    M.U.S.T. PEDICLE SCREWS SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025

    CORFLO CUBBY LOW PROFILE GASTROSTOMY DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNT·November 4, 2008

    PELVILACE T0 NEEDLE

    FDA Adverse Event
    Injury ·TISSUE SCIENCE LABORATORIES, PLC·Product code FTL·August 29, 2011

    AXON DIGITAL PREAMPLIFIER

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code GWF·July 18, 2013

    BD PEGASUS YEL 24GA X 0.75IN PRN-CAP Y

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·January 18, 2024

    M.U.S.T. SACRAL ILIAC SCREW AND PELVIC TRAUMA SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OUR·October 16, 2024

    Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F

    FDA Enforcement
    Class I ·Ongoing·Windstone Medical Packaging, Inc.·May 20, 2026