BEUDAMED
    30 results · 23ms · 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 ×

    NON-STERILE, POWDER FREE NITRILE EXAMINATION GLOVE, BLUE WITH POLYMER COATING, MODEL BLUE: ALL SIZES (XS-XL)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70607531·Sprint II - Brackets Roth .018"/.022" 20 Bracke...

    DEROYAL SURGICAL, UMBILICUP

    FDA 510(k)
    FDA Class 2 ·Hematology

    CORDIS 13F CATHETER SHEATH INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    S5 CONTROL DISPLAY MODULE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·August 8, 2012

    S5 DOUBLE HEAD PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

    S5 DOUBLE HEAD PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

    BD ULTRASAFE X100L PR CLEAR SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·July 26, 2019

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·September 26, 2019

    S5 DOUBLE HEAD PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·August 29, 2012

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·August 21, 2019

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·April 24, 2019

    ULTRASAFE X100L PR PLUM SSL NVS STEIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·October 3, 2019

    S5 CONTROL DISPLAY MODULE

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 16, 2012

    S5 CONTROL PANEL

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 15, 2012

    S5 CONTROL DISPLAY MODULE

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 16, 2012

    BD CONNECTA¿¿ PLUS STOPCOCK WITH 4-WAY 360° TAP ROTATION AND WHITE TAB

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·October 30, 2018

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 26, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP·Product code LZG·April 8, 2011

    BASE SYSTEM, ILLUMENA, NON-OEM

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO·Product code DXT·June 13, 2008