BEUDAMED
    13 results · 26ms · Sources: EU EUDAMED, US FDA

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    RAYSCAN a-Expert

    FDA 510(k)
    FDA Class 2 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517630612·CoRoent Ant TLIF Ti, 13x12x32mm 15°

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668115121·NAGAHARA/DRYSDALE MANIPULATOR DOUBLE-ENDED

    GUIDOR BIORESORBABLE MATRIX BARRIER

    FDA 510(k)
    FDA Class 2 ·Dental

    JOBST TRAVEL SOCKS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IMP,TSV,4.1,11.5,MTX,MG

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·May 18, 2021

    OT ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2018

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 18, 2011

    QUANTA SYSTEM S.P.A.

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·December 21, 2012

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·October 22, 2014

    IMP,TSV,4.1,11.5,MTX,MG

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·September 2, 2022

    DENTAL SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER DENTAL·Product code DZE·August 30, 2024

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025