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

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    RESUBMITTED RD1000 NEOPUFF INFANT RESUSCITATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTL·August 25, 2024

    C.T.M. Mobility Scooter HS-268

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    L.A.F. ISOLATION PACK

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    THERMOCOOL® SMARTTOUCH® UNI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·June 24, 2014

    ETS FLEX ARTICNG

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 8, 2010

    LAMITRODE TRIPOLE 16

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 28, 2012