BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Lumbar Interbody Fusion System (OLLIF)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111389207·MURPHY TUBE OCCLUD FCP 7"

    IRIX-A LUMBAR INTEGRATED FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARCHITECT IVANCOMYCIN

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ARCHITECT IVANCOMYCIN

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LEH·May 20, 2026

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 7, 2025

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·October 15, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 17, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 24, 2011