BEUDAMED
    28 results · 28ms · 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.
    Filters Regulation: Us FDA ×

    REPROCESSED EXTERNAL FIXATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·00304040133200·Zirlux TR D2 98x18mm

    PERFORMATRAK

    FDA UDI
    Respironics, Inc.·00606959000636·PerformaTrak Mask with Headgear, Disposable, Sm...

    Bones and Nerves 3.75mm Reusable Fiber Optic Cable

    FDA UDI
    Lumitex, Inc.·00812432022761·

    Omnilink Elite

    FDA UDI
    ABBOTT VASCULAR INC.·08717648179228·Omnilink Elite Vascular Balloon-Expandable Sten...

    Omnilink Elite

    FDA UDI
    ABBOTT VASCULAR INC.·08717648179266·Omnilink Elite Vascular Balloon-Expandable Sten...

    Omnilink Elite

    FDA UDI
    ABBOTT VASCULAR INC.·08717648179235·Omnilink Elite Vascular Balloon-Expandable Sten...

    Omnilink Elite

    FDA UDI
    ABBOTT VASCULAR INC.·08717648179259·Omnilink Elite Vascular Balloon-Expandable Sten...

    Omnilink Elite

    FDA UDI
    ABBOTT VASCULAR INC.·08717648179242·Omnilink Elite Vascular Balloon-Expandable Sten...

    Omnilink Elite

    FDA UDI
    ABBOTT VASCULAR INC.·08717648179273·Omnilink Elite Vascular Balloon-Expandable Sten...

    Claymount

    FDA UDI
    Varex Imaging Nederland B.V.·08718755000214·x-ray beam-limiting device, to restrict the dim...

    Claymount

    FDA UDI
    Varex Imaging Nederland B.V.·08718755000139·x-ray beam-limiting device, to restrict the dim...

    Varex Imaging

    FDA UDI
    Varex Imaging Nederland B.V.·08718755002232·x-ray beam-limiting device, to restrict the dim...

    Varex Imaging

    FDA UDI
    Varex Imaging Nederland B.V.·08718755001426·x-ray beam-limiting device, to restrict the dim...

    RECONSTITUTION KIT & VIAL CONNECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PURESPERM 40 AND PURESPERM 80

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

    BD SARS-COV-2 REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·June 1, 2021

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 5, 2012

    OMNILINK ELITE PERIPHERAL STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIO·September 6, 2017

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·March 20, 2013