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

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    Filters Regulation: Us FDA ×

    I-55 (methafilcon A) Soft (hydrophilic) Contact Lenses for Daily Wear

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    COMPOSIX L/P MESH WITH ECHO PS POSITIONING SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ORTHOFIX VOLAR DISTAL RADIAL PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LSLF EXT SET W CLV

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·May 24, 2013

    IN TOUCH EU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 20, 2011

    CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·August 27, 2008

    Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVD

    FDA Enforcement
    Class II ·Ongoing·Ventana Medical Systems, Inc.·August 28, 2024

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 31, 2018

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 6, 2018

    AERO LL FIXATION ANCHOR, 50MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code OVD·March 25, 2019