BEUDAMED
    293 results · 24ms · Sources: EU EUDAMED, US FDA

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    Digital Automatic Blood Pressure Monitor BPM41 Series, Digital Automatic Blood Pressure Monitor BPM45 Series

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURGI-WRAP MAST TENDON SHEET

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    COLLAGEN POWDER

    FDA 510(k)
    FDA Unclassified ·Unknown

    EVOLUTION DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·December 10, 2019

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MQR·April 7, 2022

    EVOLUTION COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MQR·June 15, 2021

    PINN CAN BONE SCREW 6.5MMX30MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS121965·Product code NDJ·October 10, 2014

    REUSABLE ACTIVE CORD

    FDA Adverse Event
    Other ·GYRUS ACMI, INC.·Product code HIH·June 10, 2011

    ASCENSIA CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·September 9, 2008

    EVOLUTION DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MUM·September 9, 2019

    EXPECT PULMONARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·January 5, 2023

    EXPECT PULMONARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·January 5, 2023

    EXPECT PULMONARY OLYMPUS 25GA - BOX 5

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·December 13, 2024

    ACQUIRE PULMONARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·February 13, 2023

    EXPECT PULMONARY OLYMPUS 22GA - BOX 5

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·February 10, 2023

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MQR·October 18, 2018

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MQR·August 20, 2020

    EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MUM·September 1, 2020

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MQR·August 20, 2020

    EVOLUTION® COLONIC CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code MQR·May 31, 2019