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

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    V. MUELLER OBSTETRICAL (OB) FORCEPS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    VORTRAN MEDICAL TECHNOLOGY 1, INC.

    FDA registration
    VORTRAN MEDICAL TECHNOLOGY 1, INC.·5 products·🇺🇸 United States

    AMBU NEUROLINE GROUND

    FDA 510(k)
    FDA Class 2 ·Neurology

    Dimension Vista LOCI Total Testosterone Flex reagent cartridge, Dimension Vista Testosterone Calibrator

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 9, 2013

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 6, 2011

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KDI·July 23, 2014

    Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·October 1, 2025