BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    MAGNETIC RESONANCE DIAGNOSTIC DEVICE

    FDA 510(k)
    FDA Class 2 ·Radiology

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909120952·REVELATION DIAMOND 811-037M - 5 PACK

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110843·TIP GUARDS VENTED ASSORTED PACK OF 100

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123113·K-WIRE - DOUBLE TROCAR 0.9mm DIA x 125mm

    ACCULIF TL-PEEK IBF CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    THE LPS - CONTINUUM TM HYBRID TIBIA, MODELS 32-5886-2Y-XX (ZIMMER) AND 05-119-XXYY1-0 (IMPLEX)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·March 24, 2022

    MULTIDIAGNOST ELEVA

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZI·May 13, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·January 11, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-REDWOOD CITY·Product code MGB·December 1, 2010