BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    MICROTENS 7757 T.E.N.S. STIMULATOR

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DD cubeY® HL

    FDA UDI
    Dental Direkt GmbH·EDDIG8440171·The DD cubeY® HL zirconium dioxide milling blan...

    CHOCOLATE AGAR W/CHEMICALLY DEFINED

    FDA 510(k)
    FDA Class 1 ·Microbiology

    FUJIFILM Endoscope Model EB-710P; FUJIFILM Processor EP-8000

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    CONSMA·Product code ITJ·June 2, 2014

    PFNA-II BLADE L90 TAN

    FDA Adverse Event
    Injury ·SYNTHES·Product code HSB·November 24, 2012

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·September 13, 2010

    Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: (1) M1501, (2) M1502, (3) M1504, (4) M15050, (5) M15151, (6) M15001, (7) M15002; Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due to an injury or disability. The device is designed for an individual lacking the ability to stand up and transfer themselves to / from a bed, the floor, a wheelchair, a chair, a toilet or similar due to reduced mobility or physical strength. Component: The deformation occurs between the bolt and the fork in the joint connecting the lifting bar and the arm on the Molift Mover.

    FDA Enforcement
    Class II ·Ongoing·ETAC A/S·February 11, 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