BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    GREINER VACUETTE BLOOD COLLECTION TUBE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623119·PEEK Corp Core, Ø12x21mm

    SAVE-SIMPLIFIED AUTOMATED VENTILATOR, MODELS: 550X10, 600X10 AND 600X12

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    T4 RIA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·January 26, 2011

    M2A-MAGNUM PF CUP 58ODX52ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 31, 2014

    THERMACHOICE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code MKN·September 6, 2007

    Philips Zenition 50, Model Number: 718096

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020