BEUDAMED
    19 results · 32ms · Sources: EU EUDAMED, US FDA

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    GENTLE LIFT-RECLINER CHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TYRX SURGICAL MESH, MODEL SMPC-0501

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

    Merge Hemo

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code FNL·June 6, 2014

    TRANSVENOUS

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 5, 2010

    TITANIUM FLETCHER-STYLE APPLICATOR SET

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS, INC.·Product code JAQ·November 27, 2012

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 25, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 25, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 25, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    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