BEUDAMED
    14 results · 23ms · Sources: EU EUDAMED, US FDA

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    Stryker Universal Mesh

    FDA 510(k)
    FDA Class 2 ·Neurology

    Oticon

    FDA UDI
    Oticon A/S·05707131305206·NERA PRO, KIT MINIRITE 312 WL DBL

    ELIA(TM) CARDIOLIPIN IGA IMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    BIOPSY VALVE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929065822·Corpectomy, 16Dx18Wx21H 0°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929036877·Corpectomy, 16Dx18Wx21H 6°

    CRYSTALLINE

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./ HUNTINGTON·Product code HQL·July 8, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 11, 2013

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 6, 2019

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·February 26, 2019

    BELIFU

    FDA Adverse Event
    Injury ·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·November 26, 2025

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·June 20, 2019