BEUDAMED
    2,945 results · 22ms · Sources: EU EUDAMED, US FDA

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    RESTORE MODULAR STERILIZATION TRAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169605060·SPACER 2131455 OLIF25 27MM 6 DEG 14X55

    ArgenIS

    FDA UDI
    ARGEN CORPORATION, THE·D818131455·MUA NC NP 3.5GH Ang30

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741314550·

    Biogel

    FDA UDI
    Bosma Enterprises·10818634023725·Biogel Skinsense Surgical 5.5 - 50 Pair/Box

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674131455060·

    Special

    FDA UDI
    Seaspine Orthopedics Corporation·10889981332037·Firefly Tap, 5.5mm

    EKO 7 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    CONKLUSION PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2014

    SORIN BCD VANGUARD BLOOD CARDIOPLEGIA SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTN·May 10, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 20, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 14, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 6, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 5, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·September 28, 2021

    PENTAX

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