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

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    MULTIFIBREN U

    FDA 510(k)
    FDA Class 2 ·Hematology

    CAMPY 5H

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DE-TOX TUBES A AND DE-TOX TUBES B

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FCG·July 16, 2014

    CONVERTBL I.V.DUAL CHANNEL HSP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 20, 2011

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·November 7, 2013

    CONVERTBL I.V..DUAL C

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·August 13, 2009

    PRIMARY PLUMSET PP YSITE 272CM NDEHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·March 19, 2012

    CONVERTBL I.V. DUAL C

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 15, 2009

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·June 3, 2015

    CONVERTBL I.V. DUAL CHANNEL HSP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·July 7, 2011

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·December 16, 2013

    LENSX LASER SYS

    FDA Adverse Event
    Injury ·ALCON - LENSX LASERS, INC.·Product code OOE·June 27, 2014

    CELL-DYN 1700 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·December 21, 2010

    SYSTEM 7 SAG SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·January 30, 2013

    UNK

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 15, 2009

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code ETN·January 14, 2015

    ENDOTRACH TUBE 8229507 CONTACT EMG 7MM

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

    NIM® EMG ELECTRODE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GXZ·January 27, 2017

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·July 1, 2016