BEUDAMED
    7 results · 35ms · 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 ×

    NOVA 13 ANALYZER, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MODELS C500/C550 ISOLETE(R) INFANT INCUBATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MUELLER TYPE FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    WAVELIGHT FS200 FEMTOSECOND LASER

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code GEX·January 17, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014

    HAKIM VALVE

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·December 9, 2010

    SINGLE USE PAPER FILTER WITH INDICATOR

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code FRG·January 30, 2019