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

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    ANTHEM Fracture System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENDOWAVE INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CHEETAH RELIANT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·December 20, 2018

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 23, 2011

    INSTINCT ENDOSCOPIC HEMOCLIP

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC.·Product code MND·June 5, 2013

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 25, 2008

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·April 1, 2019

    OPTETRAK LOGIC

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 13, 2023

    NORIAN DRILLABLE INJECT 5CC-STERILE

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MQV·June 28, 2021

    NORIAN DRILLABLE INJECT 5CC-STERILE

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MQV·April 1, 2021