BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    SURGICAL SEALANT APPLICATOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CARDIFF ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOPSY NEEDLES & TRAYS

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

    JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KNW·March 12, 2026

    INTERLOCK?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KRD·June 19, 2014

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·December 21, 2012

    TRELLIS 8 120X30

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KRA·September 21, 2010

    JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code LWE·October 8, 2025

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

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

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020