BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    ULTIMAX HAIG II NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NG-Test CARBA 5

    FDA 510(k)
    FDA Class 2 ·Microbiology

    DRX-EVOLUTION, MODEL VX3733-SYS

    FDA 510(k)
    FDA Class 2 ·Radiology

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·March 6, 2013

    VIRTUOSO VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·February 15, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·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