BEUDAMED
    37 results · 31ms · Sources: EU EUDAMED, US FDA

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    NORWOOD MEDICAL LLC

    FDA registration
    NORWOOD MEDICAL LLC·51 products·🇺🇸 United States

    CRYOPATCH SG PULMONARY TRUNK

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code DXZ·April 11, 2019

    HOVEROUND

    FDA Adverse Event
    Injury ·HOVEROUND CORPORATION·Product code ITI·July 16, 2019

    GORE-TEX VASCULAR GRAFT

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code DSY·February 5, 2009

    GORE-TEX VASCULAR GRAFT

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code DSY·February 5, 2009

    PALMAZ STENT UNKNOWN

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·May 28, 2009

    SHELHIGH

    FDA Adverse Event
    Injury ·SHELHIGH, INC.·Product code DXZ·December 18, 2007

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 8, 2013

    UNKNOWN MECHANICAL HEART VALVE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LWQ·June 24, 2022

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·March 30, 2017

    XPDM THORACIC PEDICLE PRB, ST

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code HXB·November 28, 2022

    BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 27, 2025

    BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·April 4, 2025

    PALL PXLS LEUKOCYTE REDUCTION FILTER FOR PLATELETS TRANSFUSI

    FDA Adverse Event
    Other ·PALL BIOMEDICAL PRODUCTS CO.·Product code CAK·August 29, 1997

    CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·September 3, 2021

    SFX X20 TORQUE DRIVER SHAFT

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code HWR·April 21, 2021

    SFX X20 TORQUE DRIVER SHAFT

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code HWR·November 19, 2021

    9MM POLMONIC VALVE

    FDA Adverse Event
    Death ·UNKNOWN·Product code LXA·March 28, 1996

    SFX X20 TORQUE DRIVER SHAFT

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code HWR·August 12, 2024

    EXPEDIUM SPINE SYSTEM CLIP-ON RED.DRIVER W/DOVETAIL 5.5MM

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code GEA·April 4, 2024