BEUDAMED
    7 results · 23ms · 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 ×

    R&D BATTERIES, INC. PART NUMBERS 5295, 5334, 5344 AND 5410

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AMDEN CORP.

    FDA registration
    AMDEN CORP.·4 products·🇺🇸 United States

    Airlock® osteosynthesis plate system

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CoraForce Microcatheter, CoraFlex Microcatheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 8, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·January 6, 2011

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 22, 2014