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

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    Filters Regulation: Us FDA ×

    NuVasive CoRoent Lumbar System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ProLift Trial

    FDA UDI
    Life Spine, Inc.·00190837088088·

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962102008·ETHOS PRO SMALL JOINT ANCHOR, TITANIUM, 2.9mm x...

    RADIFOCUS GLIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 22, 2018

    BIOPHEN LMWH CONTROL, LMWH CONTROL LOW, UFH CONTROL, HEPARIN CALIBRATOR & UFH CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Hematology

    MULTIFIT TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962104217·ETHOS PRO SMALL JOINT ANCHOR, TITANIUM, 2.9mm x...

    PENUMBRA SMART COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·December 11, 2015

    CONTOUR® NEXT

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code JJX·September 4, 2025

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 3, 2013

    VITALITY

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 6, 2011

    GIA 80-3.8 SINGLE USE RELOADABLE STAPLER

    FDA Adverse Event
    Injury ·PONCE - USS·Product code GDW·September 5, 2008

    CONTOUR® PLUS

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code JJX·February 20, 2025