BEUDAMED
    7 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 ×

    CANNULATED FEMORAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    THERMORITE MODEL HC-83 HYPO/HYPERTHERMIA UNIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ABUSCREEN ONTRAK FOR THC

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    TEARDROP HANDLE, AO COUPLING IMPLANT EXTRACTION SE

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 21, 2012

    KAPPA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·February 11, 2013

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    DUROM ACETABULAR COMPONENT 52/46 CODE L

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·July 16, 2014