BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Kitazato IUI Catheter

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

    SYNERGY ODM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Stern AC 3.3x10mm, Stern AC 3.3x11.5mm, Stern AC 3.3x13mm, Stern AC 4.0x8.5mm, Stern AC 4.0x10mm

    FDA 510(k)
    FDA Class 2 ·Dental

    SAPPHIRE M.T INFUSION PUMP - FRENCH

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·December 23, 2024

    UNKNOWN SAPPHIRE PUMP

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·August 6, 2025

    SAPPHIRE M.T INFUSION PUMP - FRENCH

    FDA Adverse Event
    Injury ·EITAN MEDICAL LTD.·Product code FRN·March 17, 2026

    SAPPHIRE M.T INFUSION PUMP - FRENCH

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·May 26, 2026

    UNKNOWN SAPPHIRE PUMP

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·February 2, 2026

    SAPPHIRE M.T INFUSION PUMP - GERMAN

    FDA Adverse Event
    Death ·EITAN MEDICAL LTD.·Product code FRN·April 28, 2025

    SAPPHIRE M.T INFUSION PUMP - FRENCH

    FDA Adverse Event
    Malfunction ·EITAN MEDICAL LTD.·Product code FRN·March 24, 2025

    UNKNOWN DEPUY SZ 3 10MM TIB INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC./REG. #1818910·Product code JWH·June 11, 2013

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 14, 2011

    ENDEAVOR RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·September 16, 2008