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.

    CEDIA DAU BENZODIAZEPINE ASSAY(MODIFICATION)

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    COMPUMED PULMONARY FUNCTION ANALYZER MODEL 307B

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NOVAMETRIX MODEL 510

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 11, 2013

    HUDSON SHERIDAN ENDOTRACHEAL TUBE, HVT, 5.0

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·January 5, 2011

    ENDOPATH LINEAR CUTTER RELOAD, BLACK

    FDA Adverse Event
    Malfunction ·ETHICON ENDOSURGERY·Product code GDW·July 14, 2014