BEUDAMED
    9 results · 28ms · 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.

    TEPHAFLEX SURGICAL FILM

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

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 22, 2019

    WAVEWRITER ALPHA PRIME 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 23, 2023

    ECAT VISION PET SCANNER, MODELS 3000 & 5000

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIFESITE HEMODIALYSIS ACCESS SYSTEM/CANNULA EXCHANGE, MODEL LHAS14120 & LHCEK0000

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

    INOMAX DSIR (DELIVERY SYSTEM)

    FDA Adverse Event
    Malfunction ·INOMAX MANUFACTURING LLC·Product code MRN·May 9, 2016

    PANORAMA CENTRAL STATION

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

    LIBERTY CYCLER

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·August 22, 2014

    LAMITRODE TRIPOLE 16 SURGICAL LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·April 28, 2011