BEUDAMED
    7 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.

    VRF40 VENOUS RESERVOIR WITH INTEGRAL CARDIOTOMY FILTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIASONICS TRANSVAGINAL, TV 7.5 MHZ PROBE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    STEREOTACTIC IRRADIATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011

    GIA 100-4.8 SINGLE USE RELOADABLE

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO, INC.·Product code GDW·July 19, 2014

    D&C/Cysto Pack, part number PSS3257(D

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017