BEUDAMED
    9,743 results · 42ms · 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 ×

    Spinal Electrode Kit

    FDA UDI
    Ad-Tech Medical Instrument Corporation·00841823100764·

    Mammosite Cavity Evaluation Device Kit (CED)

    FDA UDI
    Hologic, Inc.·15420045505018·MCEDII TRAY, POST-STERILE

    MAMMOSITE CAVITY EVALUATION DEVICE

    FDA Adverse Event
    Malfunction ·CYTYC SURGICAL PRODUCTS·Product code KXK·February 9, 2007

    MOMMOSITE CAVITY EVALUATION DEVICE

    FDA Adverse Event
    Injury ·CYTYC SURGICAL PRODUCTS·Product code JAQ·June 26, 2008

    ZOOM CRITICAL CARE CED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIVISION·Product code FNL·April 15, 2009

    Cook

    FDA UDI
    COOK INCORPORATED·00827002119147·Cook Esophageal Dilator Set

    Cook

    FDA UDI
    COOK INCORPORATED·00827002121188·Cook Esophageal Dilator Set

    Cook

    FDA UDI
    COOK INCORPORATED·00827002136304·Cook Esophageal Dilator Set

    Cook

    FDA UDI
    COOK INCORPORATED·00827002119130·Cook Esophageal Dilator Set

    MEMORY SOFT STONE EXTRACTOR

    FDA Adverse Event
    Injury ·WILSON-COOK·Product code FFL·July 1, 1997

    ACUSON XP

    FDA Adverse Event
    Malfunction ·ACUSON CORP.·Product code IYO·April 30, 1999

    MAMMOSITE

    FDA Adverse Event
    Malfunction ·HOLOGIC·Product code JAQ·September 15, 2010

    *

    FDA Adverse Event
    Injury ·UNK·Product code DQO·February 23, 1998

    RIATA PASSIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 10, 2013

    DEEP BRAIN STIMULATION LEAD X2

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 25, 2008

    IABP

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC.·Product code DSP·November 27, 1995

    CAPSUREFIX NOVUS MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·January 15, 2021

    CYTYC MAMMOSITE

    FDA Adverse Event
    Malfunction ·HOLOGIC LP·Product code JAQ·August 5, 2011

    CAPSURE Z NOVUS LEAD

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 3, 2021

    L-CATH PICC S/L 28GA (1.2F) X 25CM 1 LUMEN

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code LJS·May 3, 2022