BEUDAMED
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    ELMED, INC.

    FDA registration
    ELMED, INC.·83 products·🇺🇸 United States

    V MUELLER / ELMED L-HOOK CAUTERY TIP

    FDA Adverse Event
    Malfunction ·ELMED INCORPORATED·Product code GEI·November 21, 2023

    ELECTROSURGICAL UNIT

    FDA Adverse Event
    Other ·ELMED, INC.·Product code GEI·January 26, 1994

    ELMED INCORPORATED

    FDA Adverse Event
    Malfunction ·ELMED, INC.·Product code GEI·May 6, 2005

    ELMED

    FDA Adverse Event
    Other ·ELMED, INC.·Product code KNS·May 25, 1999

    SINGLE NEEDLE ENDO-CAUTERY

    FDA Adverse Event
    Malfunction ·ELMED, INC.·Product code KNS·November 3, 1994

    CUTTING ELECTRODE WITH REPLACEABLE TIP

    FDA Adverse Event
    ELMED, INC.·Product code GEI·April 2, 1993

    LAPAROSCOPIC CAUTERY HOOK

    FDA Adverse Event
    Malfunction ·ELMED INC·Product code KNS·August 31, 1998

    RETRACTOR WITH FAN BLADE

    FDA Adverse Event
    Injury ·ELMED, INC.·Product code GAD·May 15, 1995

    ADDISON II

    FDA Adverse Event
    Malfunction ·ELMED INC.·Product code GEI·October 18, 1995

    DENNIS BIPOLAR SUBMUCOSAL TURBINATE PROBE

    FDA Adverse Event
    Malfunction ·ELMED, INC.·Product code GEI·June 23, 2006

    *

    FDA Adverse Event
    Other ·ELMED, INC.·Product code HET·June 15, 2004

    ELMED

    FDA Adverse Event
    Malfunction ·ELMED INC.·Product code GEI·February 21, 1997

    MOGEN CLAMP CIRCUMCISION CLAMP

    FDA Adverse Event
    Injury ·ELMED INC.·Product code HFX·June 19, 2020

    GRASPING FORCEP

    FDA Adverse Event
    Malfunction ·ELMED, INC.·Product code KNW·May 27, 1998

    MILLENNIUM SURGICAL FIBER OPTIC RETRACTOR

    FDA Adverse Event
    Malfunction ·ELMED INC·Product code GAD·May 26, 2016

    UNK

    FDA Adverse Event
    Injury ·ELMED INC·Product code HET·April 12, 2001

    MILLENNIUM SURGICAL FIBER OPTIC RETRACTOR

    FDA Adverse Event
    Malfunction ·ELMED INC.·Product code GAD·May 27, 2016

    UNIVERSA SOFT URETERAL STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·July 15, 2016

    ENDOSCOPIC VEIN HARVESTING SYSTEM

    FDA Adverse Event
    Malfunction ·LIVANOVA USA INC·Product code GEI·July 16, 2021