BEUDAMED
    46 results · 25ms · Sources: EU EUDAMED, US FDA

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    ACIST CVi1 Contrast Delivery System, ACIST CVi Contrast Delivery System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772344123·PROTECT.PRO ACTION BACK SUPPORT BLACK L

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327424225·ISOL.ORBITAL FLOOR PLATE, SMALL,NO SLITS

    Greenwald Surgical Company, Inc.

    FDA UDI
    GRACE MANUFACTURING, INC.·10801334013325·STORZ S/S SPIKED ROLLER ELECTRODE Model # ...

    6PW - CPRotector® TWO Economy - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588030005·6PW - CPRotector® TWO Economy - Poly White

    LFRE INDIRECT LARYNGOSCOPE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OSCAR 2, MODEL 222

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    T-CONNECTOR

    FDA Adverse Event
    Malfunction ·B BRAUN·Product code FPA·January 4, 2016

    BD SYRINGE 10ML LL S/C 200

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·October 9, 2025

    LUER-LOK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·February 9, 2026

    BD LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·April 17, 2026

    AMISTEM-P

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 24, 2025

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·October 17, 2008

    CAPSURE Z NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    GYNECARE TVT SECUR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code PAH·July 2, 2013

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·December 5, 2025

    LUER-LOK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·February 9, 2026

    LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 13 MM X 45 MM Item Number: 15-2030/04

    FDA Recall
    Open, Classified ·Linkbio Corp.·Product code HSX·March 21, 2023

    BD LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·November 26, 2025

    SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSD·May 12, 2026