BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    AXOSTIM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SEAMED MODEL 6000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARGYLE JET TRACHEAL TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·July 1, 2015

    OMEGA?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·June 19, 2014

    LIFEPAK EXPRESS(R) DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 21, 2012

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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