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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    TEARLAB OSMOLARITY SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    RS BIOTECH GALAXY 'R' CO2 INCUBATOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ETHANOL ASSAY FOR THE BAYER ADVIA INTEGRATED MODULE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ENDOTRACH TUBE 8229507 CONTACT EMG 7MM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·January 7, 2014

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·November 29, 2017

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·June 16, 2017

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·December 8, 2017

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·August 30, 2016

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·May 9, 2014

    ENDOTRACHEAL TUBE 8229307 NIM EMG 7MM RE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·May 10, 2013

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·May 8, 2013

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·March 23, 2017

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·November 27, 2017

    ENDOTRACHEAL TUBE 8229306 NIM EMG 6MM RE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·May 10, 2013

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·April 21, 2016

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 9, 2025

    ACL TOP

    FDA Adverse Event
    INSTRUMENTATION LABORATORY CO.·Product code GKP·May 13, 2005

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·March 11, 2014

    ACL TOP

    FDA Adverse Event
    Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code GKP·July 21, 2005

    NIM RESPONSE® 3.0 PATIENT INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·July 22, 2014