BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    SECOND EAR BONE CONDUCTION HEARING AID

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    BONE MARROW BIOPSY SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    EMIT CAFFEINE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HANDLE WITH QUICK COUPLING, SMALL

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWX·February 10, 2021

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HET·June 16, 2006

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 11, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 10, 2011

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 23, 2014

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

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