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

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    Filters Regulation: Us FDA ×

    Precice Ankle Salvage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DELTA XTEND

    FDA UDI
    DEPUY (IRELAND)·10603295444794·DELTA XTEND HUMERAL IMPLANT DRIVER

    ELITECH CLINICAL SYSTEMS ELICAL 2; ELITECH CLINICAL SYSTEMS ELITROL I, ELITECH CLINICAL SYSTEMS ELITROL II

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    HOBBS MISTIFIER SPRAY CATHETER

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

    ABBOCATH-T 20G 1-1/4

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD·Product code FOZ·April 27, 2009

    CAPD SOLUTION TRANSFER SET (SHORT) FOR UV-FLASH

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·November 17, 2008

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·August 23, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2013

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 23, 2025

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 24, 2025

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 23, 2025

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 24, 2025

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 24, 2025