BEUDAMED
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    SEI EMG srl

    Manufacturer
    🇮🇹 Italy

    ESB 2400 SEI

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

    SEI Medical S.A. de C.V.

    FDA registration
    SEI Medical S.A. de C.V.·66 products·🇲🇽 Mexico

    SIGNATURE SE I INFUSION PUMP

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·November 21, 2019

    SIGNATURE SE I INFUSION PUMP

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·November 20, 2019

    ACUVUE OASYS FOR PRESBYOPIA

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPM·February 19, 2010

    E360 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC·Product code CBK·March 22, 2016

    COMPLETE SE STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code FGE·February 11, 2010

    X-STOP INTERSPINOUS SPACER SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQO·July 16, 2015

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·February 28, 2014

    COMPLETE SE STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code FGE·April 22, 2010

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·March 27, 2014

    COMPLETE SE ILIAC

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIO·September 17, 2013

    COMPLETE SE STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code NIO·July 28, 2010

    COMPLETE SE STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code NIO·July 1, 2010

    ACUVUE OASYS

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON VISION CARE, INC. ¿ US·Product code LPM·November 2, 2016

    REVIVE - THROMBECTOMY DEVICE

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR, LLC·Product code HCG·August 14, 2013

    CB030, 5MMX35CM EPIX LAPA SCISSOR, 10/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code HET·January 4, 2018

    ADVIA CENTAUR

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code SEI·April 15, 2026

    ATELLICA IM HBC TOTAL 2 (HBCT2)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD.·Product code SEI·March 23, 2026