BEUDAMED
    7 results · 17ms · 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.

    ASLAN KNOT PUSHER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TRUSTEEL

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 24, 2024

    MERETE DUOTHREADTM BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    A.I.M. Lead Loop Suturing Device (1), A.I.M. Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (1) plus Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (2), A.I.M. Lead Loop Suturing Device plus Tension Assist/Suture Cutter Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·February 8, 2013

    REDDICK SCOOP TIP CHOLANGIOGRAM CATHETER

    FDA Adverse Event
    Malfunction ·LEMAITRE VASCULAR·Product code GBZ·December 14, 2010

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·July 14, 2014