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

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    Secret Duo

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777600·LUMBAMED BASIC DORSAL STAY WM SILVER III

    10M - Southwest Gas Corp

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588010434·10M - Southwest Gas Corp

    SprintRay Standard Denture Base - Original Pink

    FDA UDI
    Sprintray, Inc.·00850039704246·SprintRay High Impact Denture Teeth is a light-...

    UNKNOWN NEXGEN TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·March 31, 2017

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112687·BARRON CORNEAL PUNCH 9.25MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112588·BARRON CORNEAL PUNCH 6.75MM

    SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503

    FDA 510(k)
    FDA Unclassified ·Unknown

    PELVEX HOMETRAINER

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

    BD SMARTSITE¿ VENTED VIAL ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·May 20, 2022

    BD SMARTSITE¿ VENTED VIAL ACCESS DEVICE, 13 MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code LHI·January 26, 2022

    BD SMARTSITE¿ VENTED VIAL ACCESS DEVICE, 13 MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code LHI·January 27, 2022

    UNKNOWN_SPINE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER SPINE-US·Product code NKB·April 30, 2024

    UNKNOWN_SPINE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER SPINE-US·Product code NKB·April 30, 2024

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·March 15, 2021

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·March 15, 2021

    GENDER SOLUTIONS NATURAL KNEE FLEX SYSTEM

    FDA Adverse Event
    Malfunction ·ZIMMER·Product code JWH·October 16, 2008

    DO NOT KNOW

    FDA Adverse Event
    Injury ·DO NOT KNOW·Product code FTL·August 7, 2011

    HEARTMATE II LVAS

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·June 27, 2013

    ENDURANT STENT GRAFT

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·July 21, 2020