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

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    FLEXIBLE MYOCARDIAL BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPECTRON PROXIMAL FEMORAL PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    A6 LUER ACCESS DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·June 19, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 27, 2010

    CLICKX-3D-HEAD F/PEDICSCR POST-OPEN TAN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NKB·December 21, 2012

    Philips Zenition 50, Model Number: 718096

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024