BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    TRI-LEVEL LIGAND CONTROL

    FDA 510(k)
    FDA Class 2 ·Immunology

    HEPES BUFFER IM IN NORMAL SALINE

    FDA 510(k)
    FDA Class 1 ·Hematology

    ACU-SYRINGE W/WO NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·June 10, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·October 12, 2010

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·December 10, 2012

    GLADIUS MONGO

    FDA Adverse Event
    Death ·ASAHI INTECC CO., LTD.·Product code DQX·March 22, 2024

    FIELDER FC

    FDA Adverse Event
    Death ·ASAHI INTECC CO., LTD.·Product code DQX·March 22, 2024

    GRYPHON P BR DS ANCHOR W/OC

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·January 14, 2019

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026