BEUDAMED
    6 results · 25ms · 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.

    SERIES 3 GENERAL SUCTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    QUATTRO LT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PERMANENT LEAD INTRADUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 24, 2014

    PREMIUM PLUS CEEA

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GDW·October 17, 2010

    MAXPLUS CLEAR NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·November 14, 2012