BEUDAMED
    7 results · 21ms · 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 ×

    KALGINATE IMPRESSION MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970594·anteriors; shade A2 light; mould IM

    PALMTOP VENTILATOR, MODELS PTV-8, PTV-10

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    I.B.S. osteosynthesis screws

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HUDSON NEONATE DUAL HEATED DUAL DRAIN

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code CAG·June 2, 2014

    PROFEMUR(R) Z STEM PLASMA SPRAYED

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·February 20, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 25, 2011