BEUDAMED
    10 results · 29ms · 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 ×

    MODIFICATION TO THERMOFOCUS 0800, 0900, 01500 AND 0700 SERIES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDPOR COATED TEAR DRAIN

    FDA 510(k)
    FDA Unclassified ·Unknown

    THERMO DMA DATA-CAL CALIBRATOR, MODEL 1905-050

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PRECISION MONTAGE MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 4, 2021

    WAVEWRITER ALPHA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·August 11, 2025

    VIAL ADAPTER

    FDA Adverse Event
    Malfunction ·WEST PHARMA. SERVICES, IL LTD·Product code LHI·September 22, 2022

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013

    PROFEMUR(R) NECK EXTRACTOR T-HANDLE

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LXH·April 28, 2011

    MARQUIS DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·July 10, 2008

    BD TEXIUM¿ NEEDLE-FREE SYRINGE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FMF·November 29, 2022