BEUDAMED
    25 results · 21ms · 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 ×

    POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776178888·Goodwin Sound Open Tip fr

    Bard® Goodwin Sound

    FDA UDI
    C. R. Bard, Inc.·00801741047312·Bard Goodwin Sound Open Tip 30 Fr.

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704920645·

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704266498·FRAZIER TUBE 12 FRENCH

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776080419·Frazier Suction Tube,

    PELVIC MUSCLE THERAPY

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

    LERMAN & SON CRANIAL ORTHOSIS HELMET

    FDA 510(k)
    FDA Class 2 ·Neurology

    TRIAGE D-DIMER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code GHH·May 11, 2018

    PENUMA IMPLANT

    FDA Adverse Event
    Injury ·NATIONAL MEDICAL DEVICES INC.·Product code MIB·March 1, 2018

    BARD GOODWIN SOUND

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KOE·July 16, 2020

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·May 7, 2019

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·May 7, 2019

    TRIAGE D-DIMER TEST

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·October 2, 2019

    TRIAGE D-DIMER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·September 17, 2019

    TRIAGE D-DIMER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·May 7, 2019

    TRIAGE D-DIMER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code GHH·August 17, 2018

    RUSCH 6FR 100% SILICONE FOLEY

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code KOD·April 4, 2013

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 30, 2011

    INSIGNIA ENTRA

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code DXY·May 8, 2008