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

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    Filters Regulation: Us FDA ×

    Exactech Alteon Monobloc Revision Stem

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NESSI OTC SPACER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PHARMAJET NEEDLE-FREE INJECTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD LUER-LOK¿ TIP DISPOSABLE SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 23, 2021

    DUROM US ACETABULAR COMPONENT 52/46 L

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·July 6, 2011

    VECTRIS LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·June 21, 2013

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 25, 2008