BEUDAMED
    8 results · 19ms · 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 ×

    ACETAMINOPHEN SERUM TOX EIA ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295237525·P.F.C. SIGMA CURVED TIBIAL INSERT TRIAL SZ 5 15...

    Nunchaku

    FDA 510(k)
    FDA Unclassified ·Unknown

    VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    UNI LFIT MEDIAL FEMORAL COMP.

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code HRY·April 15, 2013

    GREEN SERIES 777 INTEGRATED WALL SYSTEM

    FDA Adverse Event
    Malfunction ·WELCH ALLYN·Product code HMF·May 30, 2014

    BARDEX INFECTION CONTROL 400 SERIES TEMPERATURE-SENSING FOLE

    FDA Adverse Event
    C.R. BARD, INC.·Product code KOD·February 13, 2013

    HOME CHOICE CASSETTE C/LINEASPIGM.

    FDA Adverse Event
    Malfunction ·PLASTI ESTERIL, S.A. DE C.V.·Product code FKX·January 14, 2011