BEUDAMED
    23 results · 23ms · Sources: EU EUDAMED, US FDA

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    NuVasive CoRoent Small Ti-C System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Evolve

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215002213·

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138609·Broach, 38 X 30, 15mm Height 17° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138630·Broach, 38 X 30, 21mm Height 17° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138623·Broach, 38 X 30, 19mm Height 17° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138593·Broach, 38 X 30, 13mm Height 17° Hyperlordotic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138616·Broach, 38 X 30, 17mm Height 17° Hyperlordotic

    POWDER FREE STERILE NITRILE EXAMINATION GLOVES, BLUE; POWDER FREE POLYCHLOROPRENE STERILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ULTRASONIC TABLETOP DOPPLER; ULTRASONIC TABLETOP DOPPLER

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

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161111651380·Pelion Stem, Standard Cemented - Size 1

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161111621380·Cemented Stem, Standard Offset, Size 1

    PURITAN BENNETT 980 SERIES VENTILATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC/COVIDIEN·Product code CBK·September 17, 2025

    VITROS CHEMISTRY PRODUCTS AMON SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JID·July 14, 2011

    ZIMMER NATURAL NAIL CEPHALOMEDULLARY GUIDE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HSB·June 6, 2013

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE INC·Product code LZG·July 16, 2014

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·November 1, 2016

    PRESSIO ICP AND ICT MONITORING KIT, PARENCHYMAL WITH BOLT

    FDA Adverse Event
    Death ·SOPHYSA·Product code GWM·November 18, 2024

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 13, 2016

    PRESSIO ICP AND ICT MONITORING KIT, PARENCHYMAL WITH BOLT

    FDA Adverse Event
    Malfunction ·SOPHYSA·Product code GWM·November 18, 2024

    PRESSIO ICP AND ICT MONITORING KIT, PARENCHYMAL WITH BOLT

    FDA Adverse Event
    Malfunction ·SOPHYSA·Product code GWM·November 18, 2024