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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    HYALURONIDASE, 80 U/ML

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

    ELEKTA NEUROMAG WITH MAXFILTER

    FDA 510(k)
    FDA Class 2 ·Neurology

    INFINITY Total Ankle System, INBONE Total Ankle System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·March 6, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014