BEUDAMED
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    MVE BIOLOGICAL SOLUTIONS US LLC

    FDA registration
    MVE BIOLOGICAL SOLUTIONS US LLC·1 product·🇺🇸 United States

    MVE BIOLOGICAL SOLUTIONS US LLC

    FDA registration
    MVE BIOLOGICAL SOLUTIONS US LLC·2 products·🇺🇸 United States

    MVE Cryogenic Biological Equipment (Chengdu) Co., Ltd

    FDA registration
    MVE Cryogenic Biological Equipment (Chengdu) Co., Ltd·3 products·🇨🇳 China

    MVE

    FDA Adverse Event
    Death ·MVE, INC.·Product code ECX·October 23, 1997

    ANGIOJET

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MCX·May 21, 2020

    Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508, FRED5514, FRED3536, FRED3511, FRED5014, FRED3516, MV-F451827; FRED X 27, REF: XFRED4017-MVE, XFRED4528-MVE, MV-F501427X, XFRED4518-MVE, XFRED5526-MVE, XFRED4539-MVE, FREDX5522-PMA, FREDX3522-PMA, FREDX4525-PMA, FREDX5015-PMA, FREDX5532-PMA, FREDX4013-PMA, FREDX3513-PMA, FREDX4515-PMA, FREDX3517-PMA, MV-F352427X

    FDA Enforcement
    Class II ·Ongoing·MICROVENTION INC.·October 22, 2025

    MVE CRYO SHIPPER

    FDA Adverse Event
    Malfunction ·CHART INDUSTRIES, APPLIED TECHNOLOGIES DIVISION·Product code KSR·December 5, 2003

    CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRAL EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·July 26, 2012

    OXYLOG 3000PLUS

    FDA Adverse Event
    Malfunction ·DRÄGERWERK AG & CO. KGAA·Product code CBK·August 29, 2018

    BABYLOG VN800

    FDA Adverse Event
    Malfunction ·DRÄGERWERK AG & CO. KGAA·Product code CBK·May 21, 2026

    Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508, FRED5514, FRED3536, FRED3511, FRED5014, FRED3516, MV-F451827; FRED X 27, REF: XFRED4017-MVE, XFRED4528-MVE, MV-F501427X, XFRED4518-MVE, XFRED5526-MVE, XFRED4539-MVE, FREDX5522-PMA, FREDX3522-PMA, FREDX4525-PMA, FREDX5015-PMA, FREDX5532-PMA, FREDX4013-PMA, FREDX3513-PMA, FREDX4515-PMA, FREDX3517-PMA, MV-F352427X

    FDA Recall
    Open, Classified ·MICROVENTION INC.·Product code OUT·September 5, 2025

    KION

    FDA Adverse Event
    Malfunction ·SIEMENS-ELEMA AB LIFE SUPPORT SYSTEMS DIVISION·Product code BSZ·January 23, 2001

    ASTRAL 150 - AMER

    FDA Adverse Event
    Malfunction ·RESMED LTD·Product code NOU·March 5, 2015

    CRYOCYTE FREEZING CONTAINER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code KSE·November 13, 2003

    MVE CONSOLE, 120V, 60HZ

    FDA Adverse Event
    Injury ·BAUSCH & LOMB, INC.·Product code HQE·February 27, 2012

    LFSHLD SEC BOLD MVE

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPK·July 1, 2010

    MVE 25GA PACK WITH CUTTER

    FDA Adverse Event
    Injury ·BAUSCH & LOMB, INC.·Product code HQE·March 9, 2011

    CRYOCYTE, 50 ML W/LBL PKT.

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KSR·April 1, 2009

    OXYLOG 3000PLUS

    FDA Adverse Event
    Malfunction ·DRÄGERWERK AG & CO. KGAA·Product code CBK·December 22, 2022

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·November 18, 2015