BEUDAMED
    2,565 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.
    Filters Regulation: Us FDA ×

    KODAK INSIGHT VHC CHEST FILM

    FDA Adverse Event
    Malfunction ·KODAK HEALTH IMAGING SYSTEM, INC.·Product code IWZ·July 8, 1996

    RADIOGRAPHIC FILM

    FDA Adverse Event
    Injury ·EASTMAN KODAK CO.·Product code IWZ·September 26, 1996

    RESIUS 190 XPRES

    FDA Adverse Event
    Malfunction ·KONICA-MINOLTA MEDICAL IMAGING USA, INC.·Product code IWZ·October 13, 2009

    DF 57C DENTAL X-RAY FILM

    FDA Adverse Event
    Malfunction ·EASTMAN KODAK·Product code IWZ·September 22, 2004

    UNK

    FDA Adverse Event
    Other ·NOT AWARE THAT KODAK PRODUCT WAS INVOLVED.·Product code IWZ·December 9, 1996

    KODAK ULTRA-SPEED

    FDA Adverse Event
    Malfunction ·*·Product code IWZ·November 9, 2005

    PORTABLE RADIOGRAPHY UNIT

    FDA Adverse Event
    Malfunction ·AGFA NV·Product code IWZ·February 9, 2023

    MICROVISION CI

    FDA Adverse Event
    Malfunction ·AGFA CORP.·Product code IWZ·March 31, 2000

    RADIOLOGY FILMS

    FDA Adverse Event
    Malfunction ·*·Product code IWZ·November 15, 2004

    SILMET

    FDA Adverse Event
    Malfunction ·SILMET USA·Product code IWZ·June 10, 2002

    CRONEX ORTHO L

    FDA Adverse Event
    Malfunction ·STERLING DIAGNOSTIC IMAGING·Product code IWZ·March 24, 1998

    RADIOLOGY XR7 FILM READER/ FILM RADIOGRAPHIC

    FDA Adverse Event
    Malfunction ·KONICA MINOLTA, INC.·Product code IWZ·May 25, 2018

    SYNAPSE SOFTWARE

    FDA Adverse Event
    Malfunction ·FUJIFILM MEDICAL SYSTEMS·Product code IWZ·February 18, 2008

    Film, Radiographic

    FDA classification
    FDA Class 1 ·Film, Radiographic

    Curix Opthos H, size 35x43 cm A radiographic medical x-ray film designed to optimize diagnostic chest imaging by providing complete diagnostic information including superbly visualized lung detail along with a high level of retro-cardiac, sub-diaphragmatic and mediastinal information.

    FDA Recall
    Terminated ·AGFA Corp.·Product code IWZ·October 4, 2011

    DVB KODAK DRYVIEW --- 35x43 cm --- 125 SHT --- REF 8723132 --- Made in U.S.A. by Carestream Health, Inc., 150 Verona St, Rochester, New York 14608. General purpose radiography.

    FDA Recall
    Terminated ·Carestream Health, Inc.·Product code IWZ·December 20, 2011

    Ultra-speed Dental Film, Catalog Number/REF 834 8658, KODAK and Carestream DENTAL labels --- Carestream Health Inc.

    FDA Recall
    Terminated ·Carestream Health Inc.·Product code IWZ·July 2, 2014

    KODAK T-MAT G/RA Film, Catalog/REF # 151 0023, 24x30 cm, 5-100 Sheet Boxes FOLHAS/Hojas, Made in U.S.A. by Carestream Health, Inc. 150 Verona Street, Rochester, NY 14608 --- Device Listing # E420904 Intended use: Imaging film

    FDA Recall
    Terminated ·Carestream Health, Inc.·Product code IWZ·March 12, 2010

    Mamoray HDR-C PLUS Mammography film

    FDA Recall
    Terminated ·AGFA Corp.·Product code IWZ·February 16, 2006

    Drystar Mammo. Display of Mammographic images.

    FDA Recall
    Terminated ·AGFA Corp.·Product code IWZ·March 2, 2010