BEUDAMED
    43 results · 52ms · Sources: EU EUDAMED, US FDA

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    BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BECKER TEARDROP 5 MM, LARGE HANDLE CANNULA

    FDA Adverse Event
    Other ·BYRON MEDICAL·Product code MUU·June 3, 2010

    PERCUTANEOUS STIK

    FDA Adverse Event
    BYRON MEDICAL·Product code FMF·October 21, 1994

    5MM PATHWAY INTRODUCER

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL·Product code DYB·January 3, 2007

    ARC H-II

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL·Product code EKX·March 1, 2007

    BYRON CANDY CANE CANNULA

    FDA Adverse Event
    Other ·BYRON MEDICAL·Product code GDM·November 8, 2005

    BECKER 4MM X 26CM LARGE HANDLE CANNULA

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL·Product code MUU·December 20, 2006

    MLADICK CURVED CANNULA 4MM X 26CM

    FDA Adverse Event
    Other ·BYRON MEDICAL·Product code GDM·June 29, 2006

    BECKER 5MM X 32CM LARGE HANDLE CANNULA

    FDA Adverse Event
    Other ·BYRON MEDICAL·Product code GEA·June 21, 2006

    PSI-TEC III ASPIRATION PLATFORM 110V

    FDA Adverse Event
    Other ·BYRON MEDICAL·Product code GDM·August 7, 2009

    LYSONIX 3000 UAL SYSTEM

    FDA Adverse Event
    Injury ·BYRON MEDICAL·Product code MUU·October 14, 2011

    ACCELERATOR III 3MM X 15CM CANNULA, SMALL HAN

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL·Product code GAA·July 17, 2006

    LOCKWOOD UNDERMINER

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL, INC.·Product code GDI·March 29, 2006

    LYSONIS

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL, INC.·Product code ITX·February 5, 2004

    ARC-H II

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL INC.·Product code HWE·January 24, 2007

    PSI-TEC III INFILTRATOR

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL, INC.·Product code DQI·June 29, 2006

    BYRON

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL, INC.·Product code MUU·August 6, 2010

    LySonix 2000 Ultrasonic Surgical Systems, MODEL NO. LY-2000. --- Old labeling: MANUFACTURED BY: MISONIX, INC. EXCLUSIVELY FOR SALE BY MENTOR CORPORATION UNDER EXCLUSIVE LICENSE FROM SONIQUE SURGICAL, INC. MISONIX, INC. 1938 NEW HIGHWAY, FARMINGDALE, NY 11735. Device was manufactured from September 1996 to present.

    FDA Recall
    Terminated ·Misonix, Inc·Product code LFL·August 13, 2003

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·October 14, 2015

    PSI-TEC III ASPIRATOR

    FDA Adverse Event
    Malfunction ·BYRON MEDICAL / MENTOR TEXAS L.P.·Product code MUU·April 30, 2025