BEUDAMED
    26 results · 40ms · Sources: EU EUDAMED, US FDA

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    MotoCLIP/HiMAX Step Staple Implant System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K181166

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·December 2, 2022

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·July 15, 2020

    NUVASIVE ANTERIOR LUMBAR PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CRYOPATCH SG PULMONARY HUMAN CARDIAC PATCH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·August 17, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·May 21, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·August 12, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·June 26, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

    TRILOGY EVO, O2, BRAZIL

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·September 6, 2024

    TRILOGY EVO, BRAZIL

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·September 6, 2024

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·August 19, 2020

    SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·July 28, 2025

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 24, 2020

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 7, 2020

    CAPTURE-R READY SCREEN 3

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·July 28, 2011

    NA

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code NLM·June 17, 2013