BEUDAMED
    14 results · 20ms · 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.

    RENAL BIOPSY TRAY

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

    STEALTHSTATION SYSTEM UPDATE

    FDA 510(k)
    FDA Class 2 ·Neurology

    Force Fiber OrthoTape suture

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

    CART 9734056 S7 STAFF SHRT 100-120V INTL

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 14, 2019

    CART 9733856 S7 STAFF ASSEMBLED 110V

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 4, 2019

    NAVLOCK UNIVERSAL GREEN TRACKER

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·October 30, 2015

    SCREW DRIVER

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·August 5, 2019

    DAFILON BLUE 3/0 (2) 75CM DS39

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL S.A.·Product code GAR·March 18, 2014

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·November 29, 2012

    MEDEX NEEDLE FREE PEDIATRIC 40" CLOSED BLOOD SAMPLE KIT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code CBT·September 21, 2010

    CART 9734056 S7 STAFF SHRT 100-120V INTL

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 18, 2019

    CART 9734056 S7 STAFF SHRT 100-120V INTL

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·May 18, 2018

    NAV THORACIC PROBE TIP

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC.·Product code OLO·August 27, 2014

    NEUROLOGICAL STEREOTAXIC INSTRUMENT

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·October 26, 2015