BEUDAMED
    8 results · 26ms · 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.

    NEO-CARE DUAL LUMEN UMBILICAL CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STAR SYNC, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OPHTHALMIC FLUID DISTRIBUTION SETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HET·June 16, 2006

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 11, 2016

    PROLENE POLYPROPYLENE MESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·February 15, 2013

    SECURE ACUTE CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIV·Product code FNL·January 12, 2011

    EMAX 2 MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 13, 2013