BEUDAMED
    15 results · 21ms · Sources: EU EUDAMED, US FDA

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    EBI XFIX VISION FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENGSTROM CARESTATION, ENGSTROM PRO

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MITEK STERILIZATION TRAY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AJUST ADJUSTABLE SGL INCISION SLING

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code PAH·March 1, 2013

    HUT EXT DR FINAL ASSY-REVERSE

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code KQS·January 13, 2011

    TRANSVENE RV

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·August 8, 2014

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 30, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·November 24, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 15, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 9, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 4, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 24, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·January 12, 2026

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·March 4, 2026

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·February 19, 2026