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

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    SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00721902672279·CLAMP 961578 SURETRAK2 MEDIUM

    NA

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00763000337230·ACC 961-578 SURETRAK2 MEDIUM CLAMP

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00721902467714·CLAMP 961-578 ACC SURETRAK2 - MEDIUM

    SSP VERTEBRAL BODY REPLACEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACUSON S328, L382, L538 & L312 TRANSDUCERS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CLAMP

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

    IGS

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 3, 2019

    IGS

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

    ACC 961-578 SURETRAK2, MEDIUM CLAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code OLO·December 20, 2018

    ACC 961-578 SURETRAK2, MEDIUM CLAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code OLO·July 29, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 24, 2021

    ORTHOPAT PERIOPEATIVE AUTOTANSFUSION SYSTEM

    FDA Adverse Event
    Malfunction ·HAEMONETICS CORP.·Product code CAC·February 11, 2013

    NELLCOR OXIMAX N-600X PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code DQA·December 23, 2010

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·July 28, 2014