BEUDAMED
    52 results · 34ms · 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 ×

    neon8

    FDA UDI
    INCEREB LIMITED·05391530950077·EEG electrode array sized for use with neonatal...

    N10 NeuroBell

    FDA UDI
    INCEREB LIMITED·05391530950343·EEG electrode array, 10 electrodes, NeuroBell b...

    neon8

    FDA UDI
    INCEREB LIMITED·05391530950039·EEG electrode array sized for use with neonatal...

    Neon 12 KIT

    FDA UDI
    INCEREB LIMITED·05391530950091·Kit version of neon12, packaged without electro...

    Neon8 KIT

    FDA UDI
    INCEREB LIMITED·05391530950107·Neon8 KIT version, packaged without electrode p...

    neon12

    FDA UDI
    INCEREB LIMITED·05391530950008·EEG electrode array sized for use with neonatal...

    UNKNOWN MYNX

    FDA Adverse Event
    Injury ·CORDIS SANTA CLARA·Product code MGB·September 13, 2018

    UNKNOWN MYNX

    FDA Adverse Event
    Injury ·CORDIS SANTA CLARA·Product code MGB·September 12, 2018

    UNKNOWN MYNX

    FDA Adverse Event
    Injury ·CORDIS SANTA CLARA·Product code MGB·September 12, 2018

    TREVO XP PROVUE RETRIEVER 3X20

    FDA Adverse Event
    Injury ·CONCENTRIC MEDICAL·Product code NRY·August 4, 2017

    EMBOTRAP III 5 MM X 37 MM

    FDA Adverse Event
    Malfunction ·NEURAVI LTD.·Product code NRY·February 26, 2022

    REFLEX CATHETER

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code DQY·January 7, 2016

    SOLITAIRE FR2

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code NRY·January 4, 2016

    SOLITAIRE FR REVASCULARIZATION DEVICE

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. D/B/A EV3 NEUROVASCULAR·Product code NRY·April 1, 2016

    IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS)

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·September 21, 2016

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·April 21, 2021

    PENUMBRA SYSTEM ACE 60 REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·May 4, 2021

    NEURON MAX 6F 088 LONG SHEATH

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code DQY·September 20, 2019

    PERCLOSE PROSTYLE SUTURE-MEDIATED CLOSURE AND REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·May 22, 2023

    PENUMBRA SYSTEM JET7 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·March 3, 2021