BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    LASER-GLOBIN POWDER

    FDA 510(k)
    FDA Class 2 ·Hematology

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994726100·LID 1850094 GENERIC 3/4 IMPLANT

    Good Clean Love Personal Lubricants Almost Naked and Natural Cinnamon Vanilla

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

    LADY COMP USA

    FDA 510(k)
    FDA Unclassified ·Unknown

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 4, 2014

    ADVANTA 2 BED

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FNL·October 23, 2012

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·September 28, 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