BEUDAMED
    7 results · 27ms · 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 ×

    DTL ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DENTURE BASE RESIN

    FDA 510(k)
    FDA Class 2 ·Dental

    INFUSION SET-STERILE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 2, 2014

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·November 5, 2012

    SYNCHRON® CX5 DELTA CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JLB·September 24, 2010

    AC Powered hospital adjustable bed.

    FDA Recall
    Terminated ·Umano Medical, Inc.·Product code FNL·May 4, 2020