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 ×

    ZMR HIP SYSTEM-REVISION TAPER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GLOBAL DMSO BLASTOCYST VITRIFICATION KIT AND WARMING KIT

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

    gel-e Flex+ gel OTC

    FDA 510(k)
    FDA Unclassified ·Unknown

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 7, 2013

    CAPSUREFIX

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

    CAPSUREFIX NOVUS

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