BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    VYGON SPINAL ANESTHESIA NEEDLE W/INTRODUCER 183

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209104048·KIT, WALK - BLK

    MICROSCAN SYNERGIES PLUS GRAM POSITIVE MIC/COMBO PANELS - RIFAMPIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Wondfo CR3 Keyless Split Sample Cup

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 5, 2014

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 29, 2012

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code MGB·September 29, 2010

    Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene Liner Component (Product Line: 350-21-XX, 350-22-XX); b. Vantage Mobile-Bearing Polyethylene Liner Component (Product Line: 350-41-XX, 350-42-XX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021