BEUDAMED
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    AJ Medical Manufacturing L.L.C.

    FDA registration
    AJ Medical Manufacturing L.L.C.·1 product·🇺🇸 United States

    J CONNECTOR LOOP

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·August 10, 2020

    CADD® ADMINISTRATION SETS

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code FPA·February 6, 2017

    BD VACUTAINER® GLASS PLASMA TUBE. LT. BLUE BD HEMOGARD¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·November 27, 2017

    BD VACUTAINER® GLASS PLASMA TUBE LT. BLUE BD HEMOGARD¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·December 13, 2017

    BD MAXPLUS¿ PRESSURE RATED EXTENSION SET WITH NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·August 15, 2023

    ENDOVIVE INITIAL PLACEMENT PEG KIT, DIRECT PEJ KIT, AND PEG SAFETY KIT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·April 7, 2011

    BONE MARROW BIOPSY / ASPIRATION TRAY W/ BIOPSY & ASPIRATION NEEDLE / STERILE / L

    FDA Adverse Event
    Malfunction ·BUSSE HOSPITAL DISPOSABLES·Product code PRV·May 20, 2025

    ATW MARKER GUIDEWIRE

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DQX·April 1, 2014

    ONE-LINK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·April 29, 2026

    DENALI VENA CAVA FILTER

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·March 19, 2018

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·December 22, 2023

    ALARIS® PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·November 11, 2015

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·July 27, 2022

    USCI BAR - TEFLON GUIDE WIRE .035" CM. 3 MM "J"

    FDA Adverse Event
    Malfunction ·BARD USCI·Product code DQX·July 29, 1994

    CLEARLINK LUER ACTIVATED VALVE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·April 8, 2020

    RUNWAY GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·December 7, 2012

    TECNIS 1-PIECE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·July 25, 2017

    DENALI FEMORAL SYSTEM

    FDA Adverse Event
    Death ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·July 18, 2017

    ENROUTE TRANSCAROTID NEUROPROTECTION SYSTEM

    FDA Adverse Event
    Injury ·SILK ROAD MEDICAL·Product code NTE·October 24, 2023