BEUDAMED
    7 results · 53ms · 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 FDA Adverse Event ×

    BIPAP A40 PRO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNT·February 14, 2024

    UNICEL® DXC 600 PRO SYNCHRON® CHEMISTRY ANALYZER

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code JJE·December 27, 2010

    GE/MARQUETTE

    FDA Adverse Event
    Malfunction ·MARQUETTE·Product code DRT·August 29, 2001

    POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code LIT·November 20, 2015

    KYOCERA MEDICAL TECHNOLOGIES, INC

    FDA Adverse Event
    Malfunction ·KYOCERA MEDICAL TECHNOLOGIES, INC.·Product code OVE·April 5, 2024

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·February 5, 2016

    ARCTIC SUN® 5000

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·September 22, 2023