BEUDAMED
    8 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.
    Filters Regulation: Us FDA ×

    Celsi Monitor

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HHM

    FDA UDI
    Sbo Hearing A/S·05714464029242·HHM F500 MINIRITE T C094

    ABI Instrument, Creo Electrosurgical System

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

    BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICROCLAVE CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·October 21, 2014

    UNICEL ® DXC600I SYNCHRON ® ACCESS ® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code MMI·September 1, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 16, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025