BEUDAMED
    7 results · 19ms · 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 ×

    Mineral Collagen Composite Bioactive Extra Moldable

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NMI PICC III CATHETER, NMI HPICC III CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    XPECT GIARDIA LATERAL FLOW ASSAY, MODEL 2450020

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL·Product code OLO·October 17, 2014

    URETEX SUPPORT PP KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·July 11, 2013

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 18, 2015

    BD AUTOSHIELD¿ DUO SAFETY PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 24, 2020