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

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    Corplex P / Theracor P / Allacor P

    FDA 510(k)
    FDA Unclassified ·Unknown

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517630490·CoRoent Ant TLIF Ti, 13x11x32mm 15°

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365119910·

    QUATTRO GL SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Optomed Smartscope M5 with Optomed Smartscope FA

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    QUARTET

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·November 6, 2014

    FLEXICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 1, 2011

    GENERAL PURPOSE PROBE COVER

    FDA Adverse Event
    Injury ·ECOLAB MICROTEK MEDICAL·Product code MED·July 11, 2013

    GNS II NON-POR TIB SZ 7 RIGHT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 18, 2019

    GEN II RESURF PATELLA 38MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 19, 2019

    LEGION CR NP FEM SZ 8 RT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 18, 2019

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

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