BEUDAMED
    6 results · 16ms · 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.

    INTRADUCER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Advocate PTA Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIGITAL ULTRASOUND IMAGING SYSTEM, CONVEX ARRAY TRANSDUCER, LINEAR ARRAY TRANSDUCER, CONVEX ARRAY TRANSDUCER, PHASED ARR

    FDA 510(k)
    FDA Class 2 ·Radiology

    EDWARDS RETROFLEX 3 SHEATH

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYB·March 7, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 5, 2011

    CAPSUREFIX

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