BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    INTERPLAK

    FDA 510(k)
    FDA Class 1 ·Dental

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704920843·

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704284355·BECKMAN EATON RETRACTOR 12 1/2" 7 X 7 SHARP

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209109593·

    Exofin High Viscosity Tissue Adhesive

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

    Viewer (5.4); Elements Viewer; Mixed Reality Viewer; Smart Layout; Elements Viewer Smart Layout

    FDA 510(k)
    FDA Class 2 ·Radiology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 5, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 13, 2012

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 30, 2010

    Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1. Allura Xper FD10, Model Number: 722010. 2. Allura Xper FD10/10, Model Number: 722011. 3. Allura Xper FD20, Model Number: 722012. 4. Allura Xper FD20 Biplane, Model Number: 722013. 5. Allura Xper FD10 OR Table, Model Number: 722022. 6. Allura Xper FD20 OR Table, Model Number: 722023. 7. Allura Xper FD20 Biplane OR Table, Model Number: 722025.

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·December 18, 2024