BEUDAMED
    8 results · 24ms · 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 ×

    MEDLINE SHARPS CONTAINER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LILY VOLUME METERIC ADMINISTRATION SET, MODELS IB-2111 AND CIB-120ES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CARDIO XP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 29, 2025

    INGENUITY CT

    FDA Adverse Event
    PHILIPS MEDICAL SYSTEMS (CLEVELAND), INC.·Product code JAK·May 24, 2013

    C-REACTIVE PROTEIN (LATEX)

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code DCN·June 17, 2011

    JAGWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code EZB·August 22, 2008

    AVISTA? MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·June 26, 2025