BEUDAMED
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    ViMove2

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CARDINAL HEALTH

    FDA UDI
    Cardinal Health 200, LLC·10885380089909·1.6mm Threaded Guide Wire 150mm TiN Coated

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122261·Kwire .062x6" (1.6x150mm) Threaded

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122278·KWire .062x6" (1.6x150mm)

    COMPLEMENT C3 AND C4, SPECICAL CALIBRATOR AND SPECITROL CONTROL AND HIGH CONTROL

    FDA 510(k)
    FDA Class 2 ·Immunology

    KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK

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

    STERIS

    FDA Adverse Event
    Malfunction ·VILEX·Product code HTY·April 6, 2005

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013

    UNKNOWN DEPUY ASR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·July 8, 2011

    HUDSON NEBULIZER W/PED MASK AND TBG, SMALL VOLUM

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code CCQ·July 16, 2014

    TRUE METRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·November 21, 2019

    Allura Xper FD10/10 Product Codes: (1)722011, (2) 722027, (3) 722005; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·October 1, 2025