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

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    CSPI SPECIMEN TRAP (NON-STERILE)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Eko Model E5 System (EME5), Eko DUO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARTHRO KINETICS VESALIUS MR GENERATOR, MODELS 2004-2006; ACCESSORIES FOR MR GENERATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ASR XL ANATOMIC HEAD SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.-8010379·Product code KXA·June 12, 2014

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 15, 2010

    PROXIMATE** RELOADABLE LINEAR STAPLER - 60 MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·December 12, 2012

    VICRYL PLUS POLYGLACTIN 910 SUTURE UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·July 31, 2023

    Nussloch GmbH ASP6025 Tissue Processor

    FDA Enforcement
    Class II ·Ongoing·Leica Microsystems, Inc.·July 12, 2017