BEUDAMED
    13 results · 22ms · Sources: EU EUDAMED, US FDA

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    Disposable Nitrile Examination Glove

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113882·VISCO INJECTION CANNULA 27GA

    MT ALERT INFUSION MONITOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COMPREHENSIVE REVERSE SHOULDER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMIS 01.15.10.0190 AMIS LEG POSITIONER 2.0 FRAME

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LXH·May 17, 2022

    ACHIEVE MAPPING CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code DRF·February 2, 2018

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code MGB·September 18, 2010

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 4, 2015

    HEARTSTRING III PROXIMAL SEAL SYSTEM

    FDA Adverse Event
    Malfunction ·GUIDANT CARDIAC SURGERY·Product code DXC·October 23, 2008

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 12, 2011

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 9, 2013

    NIMBUS II FLEX AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·INFUTRONIX, LLC·Product code FRN·January 9, 2024

    BV Pulsera with Software Release 2.3-A mobile, diagnostic X-ray image acquisition and viewing system. Model Number: 718095

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 15, 2021