BEUDAMED
    28 results · 20ms · Sources: EU EUDAMED, US FDA

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    PLAYTEX EMBRACE PETITE BREAST PUMP

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

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00610131·

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70610131·Mini Sprint-Brackets 5-5 Roth .018" 200 Bracket...

    STRAIGHT PLATE, 13-HOLE

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665029048·

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193104324·HA PEEK EVOS Curved, , 13mmx11mmx 30mm , FLAT 6...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523178414·Plate Template, 12mm, Right

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523178421·Plate Template, 14mm, Right

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523178452·Plate Template, 16mm, Right

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523178407·Plate Template, 10mm, Right

    MONET ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY

    FDA 510(k)
    FDA Class 2 ·Neurology

    SMART GLOVE STERILE NITRILE EXAMINATION GLOVES (POWDERED FREE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LEG BAG WITH FLIP-FLO VALVE, FABRIC LEG STRAPS, 19 OZ., STERILE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FAQ·June 16, 2022

    MONITOR, 100CC BURETTE W/ACORN FILTER

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES PR·Product code FPA·July 20, 2006

    FREESTYLE LITE

    FDA Adverse Event
    Injury ·Product code NBW·October 29, 2010

    RU NOVOSIBIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 16, 2013

    SPINEMED TABLE - FDA 510(K) K051013

    FDA Adverse Event
    Other ·CERT HEALTH SCIENCES, LLC·Product code ITH·July 16, 2007

    ST JOSEPHS PHOENIX, AZ 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code DWF·July 31, 2009

    RU NOVOSIBRIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·April 11, 2013

    RU NOVOSIBIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DWF·October 16, 2013

    CP87170 DE MUENCHEN

    FDA Adverse Event
    Death ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011