BEUDAMED
    29 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ROSA Partial Knee System

    FDA 510(k)
    FDA Class 2 ·Neurology

    TAMPAXTAMPONSPEARLCOMPAKPEARLCOMPAKREGNORNONDO36CT

    FDA Adverse Event
    Malfunction ·TAMBRANDS MANUFACTURING, INC·Product code HEB·June 25, 2021

    Smith and Nephew

    FDA UDI
    Provision·B504TC72101210·

    CLEAR-TRAC

    FDA UDI
    Smith & Nephew, Inc.·03596010482280·CLEAR-TRAC THREADED CANNULA, 8.0 MM I.D., 76 MM...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694019743·FPS Plate Holding Tak, .062 x 6

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210151111·Resolve® Ceramic R018 UL 5-5 CS BC HK

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210151811·Resolve® Ceramic M018 UL 5-5 CS BC HK

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210151121·Resolve® Ceramic R018 UL 5-5 CS HK/MBT 4-5

    WEXLER ENDOSCOPE ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    STERILE BUTTON PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Widex

    FDA UDI
    Widex A/S·05706069914597·WIDEX MOMENT MRB2D (Titanium grey ) 110, Teleco...

    Widex

    FDA UDI
    Widex A/S·05706069827361·WIDEX EVOKE EBB3D (Titanium grey ) 110, Telecoi...

    BD MICROLANCE 3 NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·May 28, 2021

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 20, 2009

    FREESTYLE BLOOD GLUCOSE TEST STRIPS, MODELS 100-COUNT: 12401-01, 12101-21, 12101-22, 12101-23

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·October 20, 2008

    UNICEL DXC SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JGS·August 5, 2011

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 8, 2013

    MICRUSFRAME10 6MM X 11.9CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 7, 2022

    GALAXY G3 5MM X 15CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·December 7, 2022