BEUDAMED
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    ARETE MEDICAL DEVICES

    FDA registration
    ARETE MEDICAL DEVICES·1 product·🇺🇸 United States

    30 CM (12") ARBRE UNIVERSEL AMBRE AVEC 2 ACCES LUER AVEC VALVE AR ET BOUCHON

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FMG·May 23, 2024

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·May 27, 2022

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code PJS·May 27, 2022

    INTELLIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·April 2, 2018

    MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NKM·June 21, 2024

    IMPELLA CP

    FDA Adverse Event
    Death ·ABIOMED, INC.·Product code OZD·March 19, 2024

    LC BEAD

    FDA Adverse Event
    Death ·BIOCOMPATIBLES UK LTD·Product code HCG·May 27, 2016

    POWERPORT SLIM IMPLANTABLE PORT WITH ATTACHABLE 6F CHRONOFLEX OPEN-ENDED SINGLE

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code LJT·April 26, 2018

    IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both the Neuro II-SE and Neuro III-SV Magnetic Resonance Imaging Systems.

    FDA Recall
    Terminated ·Innovative Magnetic Resonance Imaging Systems Inc.·Product code LNH·October 19, 2012

    UNK LINX MAGNETIC IMPLANT

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·August 31, 2021

    RENASYS GO

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW MEDICAL LTD.·Product code OMP·April 30, 2020

    RET ROD AMBI/CL WRENCH

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KTT·April 19, 2021

    PUMP MMT-1782K 670G V4.11 MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·April 6, 2022

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·April 5, 2022

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·May 27, 2022

    ENDO GIA

    FDA Adverse Event
    Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·April 23, 2025

    630G INSULIN PUMP MMT-1715K 630G BLACK MG

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·May 12, 2020

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD/ HUNTINGTON·Product code MFK·September 3, 2010

    PUMP MMT-1780KPK 670G PATHWAY BLACK MG

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·November 8, 2021