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

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    Filters Regulation: Us FDA ×

    48CH Head Coil

    FDA 510(k)
    FDA Class 2 ·Radiology

    HYDROSOFT AND HYDROSOFT PLUS EMBOLIZATION COIL SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Neurology

    KHAN KINETIC TREATMENT (KKT-M2)

    FDA 510(k)
    FDA Unclassified ·Unknown

    WASHER 7.0MM

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HTN·February 12, 2019

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 15, 2014

    PROLIFT PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTP·June 20, 2013

    EON MINI IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 5, 2011

    INCEPTIV

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·March 10, 2026