BEUDAMED
    23 results · 22ms · Sources: EU EUDAMED, US FDA

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    THINNER RESOLVE FITNESS MONITOR/BODY SCALE, HEALTH-O-METER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890107060·Zirlux Multi-Unit Abutment 2.5 mmH compatible w...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613153170563·Drill for 6mm Screws, Dental Shaft

    neoWave C

    FDA UDI
    XENIX MEDICAL LLC·00840493415024·Rasp, Universal

    TiWAVE C Cervical Cage System

    FDA UDI
    Kalitec Direct LLC·B07320K0100060·Rasp, Universal

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0100060·Tray Insert, Lumbar Screws, 10 x 10 Assembly

    DATEX-OHMEDA AESTIVA/5 WITH 7100 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    WMT MODULAR SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADVISOR VITAL SIGNS MONITOR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL PM, INC.·Product code CCK·December 24, 2008

    AISYS

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·January 15, 2016

    ADVISOR VITAL SIGNS MONITOR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL PM, INC·Product code DQK·April 28, 2010

    BD INSYTE AG BC GLOBAL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 22, 2024

    BD INSYTE AG BC GLOBAL WING

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 29, 2024

    BD INSYTE AG BC GLOBAL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 13, 2024

    BD IAG BC PRO GLOBAL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 4, 2025

    ENDO GIA ULTRA UNIVERSAL STAPLER

    FDA Adverse Event
    Other ·COVIDIEN·Product code GDW·March 12, 2013

    ENDURON NEUT 52OD X 28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·February 11, 2011

    RIATA ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008

    Meridian ST Femoral Stem

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code MAY·August 24, 2005

    REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring.

    FDA Enforcement
    Class II ·Terminated·LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC·March 7, 2018