BEUDAMED
    6 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.

    THROMBELASTOGRAPH COAGULATION ANALYZER 3000S

    FDA 510(k)
    FDA Class 2 ·Hematology

    CHURCHILL-H VENTED IV SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ARGENCO 19

    FDA 510(k)
    FDA Class 2 ·Dental

    2.5MM HEX SCREWDRIVER-LONG

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code HXX·February 11, 2013

    MYNX VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·January 10, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 24, 2014