BEUDAMED
    7 results · 20ms · 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 ×

    KRONUS KALIBRE THYROID PEROXIDASE ANTIBODY EIA KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    SWAN-GANZ FLOW DIRECTED PRESSURE TD CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VITEK GRAM NEGATIVE IDENTIFICATION CARD, MODIFIED

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·January 6, 2020

    2008K2 HEMODIALYSIS MACHINE

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code KDI·June 5, 2014

    STORAGE TRAY CLIPS APPLIER/INSTRUMENTS

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code LRP·January 9, 2013

    SYMPHONY

    FDA Adverse Event
    Malfunction ·SORIN CRM·Product code NVZ·November 4, 2010