BEUDAMED
    9 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 ×

    Electrically Powered Wheelchair

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    IMP,TSV,4.1MM,SBM,10

    FDA Adverse Event
    Malfunction ·ZIMMER DENTAL·Product code DZE·March 17, 2022

    ReBorn (1050nm)

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

    Crossloop

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMP,TSV,4.1MM,SBM,10

    FDA Adverse Event
    Malfunction ·ZIMMER DENTAL·Product code DZE·May 20, 2022

    RX CYTOLOGY BRUSH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FDX·November 11, 2014

    UNICEL DXL 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·August 19, 2011

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 23, 2013

    ABX MINOTROL 16

    FDA Adverse Event
    Other ·HORIBA MEDICAL·Product code GKZ·June 6, 2013