BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    DERMATOPHYTE TEST MEDIUM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Tranquil-L™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788221310·Steerable Graft Tamp

    EasyTouch

    FDA UDI
    MHC MEDICAL PRODUCTS, LLC·MHC18221311·

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011822131200·Ortho-Cast Buccal tubes M-Series 22,-14°Torque ...

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011822131100·Ortho-Cast Buccal tubes M-Series 22,-14°Torque...

    NB 1 SA Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    POWDER FREE NITRILE EXAMINATION GLOVE-BLUE (CHEMOTHERAPY)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRAL EASE PERICARDIAL BIOPROSTHESES

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·May 20, 2014

    PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012

    FEMOSTOP

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL·Product code DXC·August 20, 2010

    TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;

    FDA Enforcement
    Class II ·Ongoing·D.O.R.C. Dutch Opthalmic Research Center Intl B.V.·June 17, 2026