BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    ATLAS ORTHOGONAL PERCUSSION INSTTUMENT

    FDA 510(k)
    FDA Unclassified ·Unknown

    VARIAX

    FDA UDI
    Stryker GmbH·04546540540805·Inlay, 1.2XS,1.7S Hand Standard Plates

    DATEX-OHMEDA PRESTIN MODULE (MODEL FAMILY E-PRESTIN, INCLUDING E-PRESTIN, E-RESTIN, E=PRETIN, E-PP AND E-PT/E-P)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SmartGuard technology; Predictive Low Glucose technology

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    OT VERIO IQ METER

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

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 6, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code CAW·July 22, 2014