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

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    VitruvianScan (v1.0)

    FDA 510(k)
    FDA Class 2 ·Radiology

    LCP

    FDA UDI
    Synthes GmbH·10886982167729·3.5MM LCP® PROXIMAL HUMERUS PLATE-LONG 12H SHAF...

    Burr

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113158·DIAMOND BURR 5.0MM DIAMETER BALL

    TOTAL PROTEIN URINE/CSF GEN.3

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ST360 SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JDEVOLUTION S

    FDA Adverse Event
    Injury ·J DENTAL CARE SRL·Product code DZE·November 11, 2025

    JDEVOLUTION PLUS

    FDA Adverse Event
    Injury ·J DENTAL CARE SRL·Product code DZE·February 4, 2026

    CELL-DYN EMERALD

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·September 9, 2011

    2520274-2013-04584

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 22, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 22, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·May 2, 2016