BEUDAMED
    6 results · 18ms · 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.

    TRICON REVISION TOTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INNOFLUOR PHENYTOIN

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ASPARTATE AMINOTRANSFERASE REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SURFLASH PLUS SAFETY IV CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION - KOFU·Product code FOZ·June 3, 2014

    HUDSON ISIS SUBGLOTTIC ET TUBE, 6.0

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·November 8, 2012

    TIBIAL BASEPLATE M-2?

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code JWH·September 20, 2010