BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ArgenPMMA Multi98x30-D3

    FDA UDI
    ARGEN CORPORATION, THE·D818123297·Crown And Bridge, Temporary, Resin

    MEDLINE FOG INHIBITOR WITH SPONGE NONFB100

    FDA Adverse Event
    Malfunction ·ASPEN SURGICAL PRODUCTS, CALEDONIA·Product code OCT·June 14, 2017

    REDONDO-L

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    URS-1B (BLOOD TEST)

    FDA 510(k)
    FDA Class 2 ·Hematology

    INFLATOR KIT 18INFKIT BALLOON

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code LRC·August 15, 2014

    BALLOON SEEKER

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code LRC·August 15, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 21, 2013

    TRIDENT 0° X3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·September 26, 2014

    PIN COLLET

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code GET·June 8, 2011

    ACTIVA PC

    FDA Adverse Event
    Malfunction ·MPROC, JUNCOS·Product code MHY·July 13, 2009