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

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    QBC(R) CENTRIFUGAL HEMATOLOGY CONTR/MULTI MODIFIED

    FDA 510(k)
    FDA Class 2 ·Hematology

    OptoWire III

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NOBELPROCERA IMPLANT BRIDGE ZIRCONIA

    FDA 510(k)
    FDA Class 2 ·Dental

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 7, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 27, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 16, 2018

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 24, 2014

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 5, 2010

    ENDURANT II ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·December 31, 2012

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 5, 2018

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026

    Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in the USA by Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The T2 Arthrodesis Nail is intended for the treatment of Knee Arthrodesis. The design of the T2 Arthrodesis Nail features a unique curvature which incorporates both femur ante curvature and knee valgus bend. Indications: Aseptic failed total knee arthro-plasty with or without bone loss; Failed external fixation, non unions and malunions; Periarticular fractures where repair is not possible; Pathologic fractures and tumor resections; Pseudoarthrosis and correct osteotomy; Ipsilateral femur fractures; and Open and closed femoral fractures.

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·July 25, 2012