BEUDAMED
    7 results · 22ms · 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 ×

    mi-eye 2, mi-eye 2 monitor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LMA STONEBREAKER DEVICE; PROBE SIZE 1.0MM, 1.6MM, 2.0MM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    XTRACT SYRINGE KEY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STONEBREAKER SINGLE USE PROBE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FFK·March 28, 2018

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 14, 2011

    HEARTSTREAM FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 6, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014