BEUDAMED
    6 results · 17ms · 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(12 FR) LPS 5213/MODIFIED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ST-E1 OVERTUBE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PLASTIC-GUIDES

    FDA 510(k)
    FDA Class 1 ·Radiology

    OT VERIO IQ METER

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

    PROXIMAL INTERPHALANGEAL JOINT PYROCARBON IMPL

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS·Product code NEG·November 22, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

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