BEUDAMED
    18 results · 24ms · Sources: EU EUDAMED, US FDA

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    G-Vitri™ Vitrification Straw

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

    ADULT ENDOTRACHEAL CLOSED SUCTION SYSTEM 24 HOURS, SIZE 16F

    FDA UDI
    Intersurgical Incorporated·05030267097814·ADULT ENDOTRACHEAL CLOSED SUCTION SYSTEM 24 HOU...

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517195166·MaXcess 4 Removal Tool, Locking Shim

    Histofluor® Rodent LKS Fluorescent Antibody Test System

    FDA UDI
    IMMUNO CONCEPTS INC·M74912400021·Mouse LKS Tissue Kit - 400 tests

    ARKEO, Wedge Fixation System

    FDA UDI
    Auxano Medical LLC·00850055649712·ARKEO Wedge Draw Rod Assy

    Endoscopic Biopsy Forceps

    FDA UDI
    MEDTRONIC PS MEDICAL, INC.·00643169497740·FORCEPS 3240-002 GRASPING 2MM L 28.5

    Forceps, Grasping, Down, 2mm, 28.5cm

    FDA UDI
    CLARUS MEDICAL, LLC·10810004820781·Forceps, Grasping, Down, 2mm, 28.5cm

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR32400021·SARA Distance ring 2 mm

    2.7 X 100mm OLIVE PIN SS

    FDA UDI
    Osteocentric Technologies, Inc.·00810189110304·2.7 X 100mm OLIVE PIN SS

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR32400020101·SARA Distance ring 2 mm

    MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP3AX1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Anterior Spine Truss System – Stand Alone (ASTS-SA) Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FORCEPS, 2MM GRASPING

    FDA Adverse Event
    Other ·CLARUS MEDICAL, LLC.·Product code HTD·September 22, 2004

    AMS 800 URINARY CONTROL SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EZY·April 24, 2019

    . FLO-GARD 6301 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·November 24, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 8, 2011

    TOTALCARE BARIATRIC PLUS BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·July 11, 2013

    Boston Scientific TELIGEN, Implantable Cardiac Defibrillator models E102, E110, the following models are not available in the US: models F102, F110, F111. Sterilized using ethylene oxide. Boston Scientific, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. Indicated for patients who are at risk for sudden cardiac death due to ventricular arrhythmias and may require pacing support.

    FDA Enforcement
    Class II ·Terminated·Boston Scientific CRM Corp·October 23, 2013