BEUDAMED
    9 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.

    OMNIMED NASAL OXYGEN CANNULA

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902709487·EXTRAS SET - HALF SIZE CASE

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376319872·Occipital Plate, 66mm

    RECIPROC BLUE FILES, 6X, STERILE

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·May 13, 2024

    Exactech Alteon Monobloc Revision Stem

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    C-CO2 COLORIMETRIC CO2 INDICATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TOTAL ASR ACET IMP SIZE 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·June 4, 2014

    SINGLE EXTENSION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 26, 2012

    EXCELCARE BARIATRIC BED FRAME

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC·Product code FNL·September 28, 2010