BEUDAMED
    10 results · 34ms · 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.

    WHEELED STRETCHER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295238409·P.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ ...

    SIGMA 5000 SERIES, IMAGIC

    FDA 510(k)
    FDA Class 2 ·Radiology

    VITEK 2 AST Gram Negative Cefotaxime (<=0.25 - >=64 ug/mL)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CDS/R/4K DILUENT/SHEATH, 20L

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·April 12, 2007

    CD SAPPHIRE, CD 4000 SYSTEMS DILUENT/SHEATH

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·December 8, 2006

    CELL-DYN DILUENT/SHEATH

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKL·January 5, 2007

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 18, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 28, 2014

    HIRES 90K

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS, LLC·Product code MCM·January 5, 2011