BEUDAMED
    7 results · 18ms · 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.

    STRATO PORT INTRODUCER KT(10 FR) LPS 5057/MODIFIED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACL CROSSPIN

    FDA UDI
    Biomet Orthopedics, LLC·00880304407657·

    (EIA) FOR IGM ANTIBODY TO EBV VCA IN HUMAN SERUM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    GIANT LUMEN SAFETIP SERIES: ENDOMYOCARDIAL BIOPSY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

    N/A

    FDA Adverse Event
    Malfunction ·ASCENT·Product code NLQ·November 23, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 1, 2014