BEUDAMED
    47 results · 35ms · Sources: EU EUDAMED, US FDA

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    Medtronic Bio-Medicus Adult Cannula Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CS 2200

    FDA UDI
    CARESTREAM DENTAL LLC·60192155153594·CS 2200 110V/205CM LONG WALL MTD

    CS 2200

    FDA UDI
    CARESTREAM HEALTH, INC.·60889975153599·CS 2200 110V/205CM LONG WALL MTD

    POWER-LOAD COT FASTENER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PROPHECY PRE-OPERATIVE NAVIGATION ALIGNMENT GUIDES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·February 20, 2020

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·April 29, 2026

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·April 8, 2026

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·March 11, 2026

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 26, 2026

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·March 5, 2026

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 19, 2026

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 19, 2026

    RIATA ST OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·October 8, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 8, 2013

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 7, 2011

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 18, 2026

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·April 7, 2026

    BD CONNECTA PLUS3 BLUE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·June 19, 2024

    CARDIOHELP

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 21, 2026